more general categories |
information about this item |
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1. Human Genes |
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1. Human Genes |
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cytochrome P450, family 11, subfamily A, polypeptide 01 [HGNC:CYP11A1] (65) |
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cytochrome P450, family 19, subfamily A, polypeptide 01 [HGNC:CYP19A1] (210) |
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estrogen receptor 1 [HGNC:ESR1] (506) |
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progesterone receptor [HGNC:PGR] (209) |
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hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 [HGNC:HSD3B2] (55) |
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sulfotransferase family 1E, estrogen-preferring, member 1 [HGNC:SULT1E1] (49) |
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sulfotransferase family, cytosolic, 2A, dehydroepiandrosterone (DHEA)-preferring, member 1 [HGNC:SULT2A1] (47) |
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2. Interaction: Human Genes and Chemicals |
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2. Interaction: Human Genes and Chemicals |
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binding (2423) |
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activity (2549) |
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expression (2187) |
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activity (2865) |
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expression (3238) |
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A. Anatomy |
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A. Anatomy |
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Peters anomaly [MESH:C537884] (465) |
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C02. Virus Diseases |
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C02. Virus Diseases |
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Hepatitis C [MESH:D006526] (1627) |
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Hepatitis C [MESH:D006526] (1627) |
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C04. Neoplasms |
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C04. Neoplasms |
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Precancerous Conditions [MESH:D011230] (2858) |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
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Liposarcoma, Myxoid [MESH:D018208] (358) |
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Leiomyoma [MESH:D007889] (744) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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Liposarcoma, Myxoid [MESH:D018208] (358) |
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Glioblastoma [MESH:D005909] (2554) |
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Melanoma [MESH:D008545] (3508) |
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ACTH-Secreting Pituitary Adenoma [MESH:D049913] (169) |
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Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
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Mesothelioma [MESH:D008654] (2567) |
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Prolactinoma [MESH:D015175] (312) |
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Carcinoma, Transitional Cell [MESH:D002295] (2662) |
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Carcinoma, Adenoid Cystic [MESH:D003528] (1561) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Prostatic Intraepithelial Neoplasia [MESH:D019048] (1565) |
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Bowen's Disease [MESH:D001913] (247) |
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Mesothelioma [MESH:D008654] (2567) |
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Glioblastoma [MESH:D005909] (2554) |
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Papilloma [MESH:D010212] (2243) |
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Bowen's Disease [MESH:D001913] (247) |
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Meningioma [MESH:D008579] (978) |
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Glioblastoma [MESH:D005909] (2554) |
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Melanoma [MESH:D008545] (3508) |
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Multiple Myeloma [MESH:D009101] (2767) |
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Hemangiosarcoma [MESH:D006394] (1836) |
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Meningioma [MESH:D008579] (978) |
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Melanoma [MESH:D008545] (3508) |
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Skin Neoplasms [MESH:D012878] (2992) |
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Breast Neoplasms, Male [MESH:D018567] (650) |
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Esophageal Neoplasms [MESH:D004938] (3737) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Ovarian Neoplasms [MESH:D010051] (3275) |
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ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172) |
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Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
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Prolactinoma [MESH:D015175] (312) |
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Esophageal Neoplasms [MESH:D004938] (3737) |
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Salivary Gland Neoplasms [MESH:D012468] (968) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Pituitary Neoplasms [MESH:D010911] (914) |
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Meningioma [MESH:D008579] (978) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm Metastasis [MESH:D009362] (4441) |
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Neoplasm Recurrence, Local [MESH:D009364] (1949) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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C05. Musculoskeletal Diseases |
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C05. Musculoskeletal Diseases |
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Bone Resorption [MESH:D001862] (2352) |
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Acromegaly [MESH:D000172] (466) |
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Osteoporosis [MESH:D010024] (3037) |
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C06. Digestive System Diseases |
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C06. Digestive System Diseases |
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Cholestasis [MESH:D002779] (3419) |
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Barrett Esophagus [MESH:D001471] (1930) |
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Esophageal Neoplasms [MESH:D004938] (3737) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Barrett Esophagus [MESH:D001471] (1930) |
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Esophageal Neoplasms [MESH:D004938] (3737) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Crohn Disease [MESH:D003424] (2585) |
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Esophageal Neoplasms [MESH:D004938] (3737) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Colitis, Ulcerative [MESH:D003093] (2601) |
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Crohn Disease [MESH:D003424] (2585) |
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Cecal Neoplasms [MESH:D002430] (822) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Colorectal Neoplasms [MESH:D015179] (4534) |
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Stomach Neoplasms [MESH:D013274] (4942) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Non-alcoholic Fatty Liver Disease [MESH:C541083] (1567) |
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Hepatitis C [MESH:D006526] (1627) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Liver Cirrhosis, Experimental [MESH:D008106] (4589) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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Carcinoma, Hepatocellular [MESH:D006528] (5375) |
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Pancreatitis [MESH:D010195] (1924) |
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C07. Stomatognathic Diseases |
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C07. Stomatognathic Diseases |
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Salivary Gland Neoplasms [MESH:D012468] (968) |
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Salivary Gland Neoplasms [MESH:D012468] (968) |
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C08. Respiratory Tract Diseases |
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C08. Respiratory Tract Diseases |
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Pulmonary Fibrosis [MESH:D011658] (3140) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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Carcinoma, Non-Small-Cell Lung [MESH:D002289] (3540) |
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C09. Otorhinolaryngologic Diseases |
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C09. Otorhinolaryngologic Diseases |
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Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
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C10. Nervous System Diseases |
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C10. Nervous System Diseases |
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Not Fully Specified [NFS] (4027) |
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Demyelinating Diseases [MESH:D003711] (2917) |
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Pituitary Neoplasms [MESH:D010911] (914) |
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Brain Ischemia [MESH:D002545] (4873) |
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Alzheimer Disease [MESH:D000544] (4275) |
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Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54) |
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Seizures [MESH:D012640] (4502) |
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Migraine Disorders [MESH:D008881] (2318) |
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Pituitary Neoplasms [MESH:D010911] (914) |
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Hypopituitarism [MESH:D007018] (732) |
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Acromegaly [MESH:D000172] (466) |
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ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172) |
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Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
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Prolactinoma [MESH:D015175] (312) |
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Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54) |
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Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
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Pituitary Neoplasms [MESH:D010911] (914) |
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Meningioma [MESH:D008579] (978) |
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von Hippel-Lindau Disease [MESH:D006623] (580) |
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Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
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Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
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Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54) |
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Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
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Alzheimer Disease [MESH:D000544] (4275) |
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Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54) |
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Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54) |
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Seizures [MESH:D012640] (4514) |
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Muscular Atrophy [MESH:D009133] (1234) |
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Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
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Hyperalgesia [MESH:D006930] (3929) |
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Peripheral Nervous System Diseases [MESH:D010523] (6151) |
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Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54) |
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Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
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C11. Eye Diseases |
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C11. Eye Diseases |
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Peters anomaly [MESH:C537884] (465) |
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Peters anomaly [MESH:C537884] (465) |
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Glaucoma 3, Primary Congenital, A [MESH:C565547] (434) |
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Glaucoma, Primary Open Angle [MESH:C562750] (466) |
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Glaucoma 1, Open Angle, A [MESH:C564234] (446) |
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C12. Male Urogenital Diseases |
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C12. Male Urogenital Diseases |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Aromatase deficiency [MESH:C537436] (277) |
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Oligospermia [MESH:D009845] (799) |
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Hypospadias 1, X-Linked [MESH:C567482] (571) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Aromatase deficiency [MESH:C537436] (277) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Adrenal hyperplasia 2 [MESH:C538236] (89) |
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Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
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Sexual Infantilism [MESH:D050035] (277) |
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Hypospadias 1, X-Linked [MESH:C567482] (571) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Diabetic Nephropathies [MESH:D003928] (2301) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Glomerulonephritis [MESH:D005921] (3758) |
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Kidney Tubular Necrosis, Acute [MESH:D007683] (974) |
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Kidney Failure, Chronic [MESH:D007676] (2930) |
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Pseudohypoaldosteronism [MESH:D011546] (232) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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C13. Female Urogenital Diseases and Pregnancy Complications |
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C13. Female Urogenital Diseases and Pregnancy Complications |
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Not Fully Specified [NFS] (1116) |
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Endometriosis [MESH:D004715] (2461) |
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Ovarian Neoplasms [MESH:D010051] (3281) |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Infertility, Female [MESH:D007247] (2184) |
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Aromatase deficiency [MESH:C537436] (277) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Adrenal hyperplasia 2 [MESH:C538236] (89) |
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Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
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Sexual Infantilism [MESH:D050035] (277) |
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Hypospadias 1, X-Linked [MESH:C567482] (571) |
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Ovarian Neoplasms [MESH:D010051] (3281) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Diabetic Nephropathies [MESH:D003928] (2301) |
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Carcinoma, Renal Cell [MESH:D002292] (2975) |
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Glomerulonephritis [MESH:D005921] (3758) |
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Kidney Tubular Necrosis, Acute [MESH:D007683] (974) |
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Kidney Failure, Chronic [MESH:D007676] (2930) |
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Pseudohypoaldosteronism [MESH:D011546] (232) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Abortion, Spontaneous [MESH:D000022] (2780) |
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Diabetes, Gestational [MESH:D016640] (1157) |
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C14. Cardiovascular Diseases |
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C14. Cardiovascular Diseases |
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Not Fully Specified [NFS] (2667) |
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Heart Failure [MESH:D006333] (4058) |
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Cardiomyopathy, Dilated [MESH:D002311] (1576) |
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Cardiomyopathy, Dilated [MESH:D002311] (1576) |
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Diabetic Cardiomyopathies [MESH:D058065] (1995) |
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Myocardial Infarction [MESH:D009203] (4122) |
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Coronary Artery Disease [MESH:D003324] (2685) |
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Ventricular Dysfunction, Left [MESH:D018487] (1631) |
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Reperfusion Injury [MESH:D015427] (4968) |
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von Hippel-Lindau Disease [MESH:D006623] (580) |
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Atherosclerosis [MESH:D050197] (4188) |
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Coronary Artery Disease [MESH:D003324] (2685) |
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Brain Ischemia [MESH:D002545] (4873) |
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Multiple Myeloma [MESH:D009101] (2765) |
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Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy [MESH:C565359] (84) |
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Hypertension, Malignant [MESH:D006974] (621) |
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Myocardial Infarction [MESH:D009203] (4151) |
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Coronary Artery Disease [MESH:D003324] (2685) |
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C15. Hemic and Lymphatic Diseases |
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C15. Hemic and Lymphatic Diseases |
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Multiple Myeloma [MESH:D009101] (2765) |
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Multiple Myeloma [MESH:D009101] (2765) |
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Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
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C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
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Peters anomaly [MESH:C537884] (465) |
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Aromatase deficiency [MESH:C537436] (277) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Adrenal hyperplasia 2 [MESH:C538236] (89) |
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Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
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Sexual Infantilism [MESH:D050035] (277) |
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Hypospadias 1, X-Linked [MESH:C567482] (571) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Adrenal hyperplasia 2 [MESH:C538236] (89) |
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Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
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Hypospadias 1, X-Linked [MESH:C567482] (571) |
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Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
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Bulbospinal neuronopathy, X-linked recessive [MESH:C537017] (565) |
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Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
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Aromatase deficiency [MESH:C537436] (277) |
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Hyperlipidemia, Familial Combined [MESH:D006950] (372) |
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Hyperlipoproteinemia Type I [MESH:D008072] (219) |
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Hyperlipoproteinemia Type II [MESH:D006938] (707) |
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Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
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Pseudohypoaldosteronism [MESH:D011546] (232) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Adrenal hyperplasia 2 [MESH:C538236] (89) |
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Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
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C17. Skin and Connective Tissue Diseases |
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C17. Skin and Connective Tissue Diseases |
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Skin Neoplasms [MESH:D012878] (2991) |
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Breast Neoplasms, Male [MESH:D018567] (650) |
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Aromatase deficiency [MESH:C537436] (277) |
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Alopecia [MESH:D000505] (1453) |
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C18. Nutritional and Metabolic Diseases |
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C18. Nutritional and Metabolic Diseases |
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Hyperglycemia [MESH:D006943] (1858) |
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Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
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Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
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Diabetes, Gestational [MESH:D016640] (1152) |
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Insulin Resistance [MESH:D007333] (3511) |
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Hypercholesterolemia [MESH:D006937] (1404) |
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Hyperlipidemia, Familial Combined [MESH:D006950] (372) |
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Hypertriglyceridemia [MESH:D015228] (808) |
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Hyperlipoproteinemia Type I [MESH:D008072] (219) |
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Hyperlipoproteinemia Type II [MESH:D006938] (707) |
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Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
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Aromatase deficiency [MESH:C537436] (277) |
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Hyperlipidemia, Familial Combined [MESH:D006950] (372) |
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Hyperlipoproteinemia Type I [MESH:D008072] (219) |
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Hyperlipoproteinemia Type II [MESH:D006938] (707) |
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Ceroid lipofuscinosis, neuronal 1, infantile [MESH:C537948] (946) |
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Pseudohypoaldosteronism [MESH:D011546] (232) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Adrenal hyperplasia 2 [MESH:C538236] (89) |
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Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
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Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54) |
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Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54) |
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Hyperkalemia [MESH:D006947] (485) |
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Hypokalemia [MESH:D007008] (1041) |
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Obesity [MESH:D009765] (4462) |
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C19. Endocrine System Diseases |
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C19. Endocrine System Diseases |
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Adrenal Insufficiency [MESH:D000309] (1599) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Adrenal hyperplasia 2 [MESH:C538236] (89) |
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Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
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Diabetes, Gestational [MESH:D016640] (1152) |
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Diabetes Mellitus, Experimental [MESH:D003921] (4771) |
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Diabetes Mellitus, Type 2 [MESH:D003924] (4219) |
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Diabetic Cardiomyopathies [MESH:D058065] (1995) |
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Diabetic Nephropathies [MESH:D003928] (2301) |
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Ovarian Neoplasms [MESH:D010051] (3275) |
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ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172) |
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Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
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Prolactinoma [MESH:D015175] (312) |
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Puberty, Precocious [MESH:D011629] (1147) |
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Aromatase deficiency [MESH:C537436] (277) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Androgen-Insensitivity Syndrome [MESH:D013734] (567) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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Adrenal hyperplasia 2 [MESH:C538236] (89) |
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Adrenal hyperplasia, congenital, type 5 [MESH:C538237] (223) |
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Sexual Infantilism [MESH:D050035] (277) |
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Sexual Infantilism [MESH:D050035] (277) |
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Ovarian Neoplasms [MESH:D010051] (3281) |
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Polycystic Ovary Syndrome [MESH:D011085] (2186) |
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Hyperparathyroidism [MESH:D006961] (1475) |
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Hypopituitarism [MESH:D007018] (732) |
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Acromegaly [MESH:D000172] (466) |
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ACTH-Secreting Pituitary Adenoma [MESH:D049913] (172) |
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Growth Hormone-Secreting Pituitary Adenoma [MESH:D049912] (383) |
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Prolactinoma [MESH:D015175] (312) |
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C20. Immune System Diseases |
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C20. Immune System Diseases |
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Multiple Myeloma [MESH:D009101] (2767) |
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Leukemia, Lymphocytic, Chronic, B-Cell [MESH:D015451] (2562) |
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Multiple Myeloma [MESH:D009101] (2765) |
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C22. Animal Diseases |
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C22. Animal Diseases |
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Disease Models, Animal [MESH:D004195] (2058) |
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Mammary Neoplasms, Animal [MESH:D015674] (2735) |
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C23. Pathological Conditions, Signs and Symptoms |
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C23. Pathological Conditions, Signs and Symptoms |
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Alopecia [MESH:D000505] (1383) |
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Muscular Atrophy [MESH:D009133] (1234) |
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Hernia, Diaphragmatic [MESH:D006548] (2647) |
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Cardiomegaly [MESH:D006332] (3802) |
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Intestinal Polyps [MESH:D007417] (1592) |
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Fibrosis [MESH:D005355] (3133) |
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Hyperplasia [MESH:D006965] (2463) |
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Necrosis [MESH:D009336] (4019) |
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Nerve Degeneration [MESH:D009410] (4061) |
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Critical Illness [MESH:D016638] (296) |
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Disease Progression [MESH:D018450] (2868) |
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Recurrence [MESH:D012008] (830) |
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Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
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Amenorrhea [MESH:D000568] (817) |
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Oligomenorrhea [MESH:D009839] (228) |
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Neoplasm Invasiveness [MESH:D009361] (3388) |
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Neoplasm Metastasis [MESH:D009362] (4441) |
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Neoplasm Recurrence, Local [MESH:D009364] (1949) |
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Cell Transformation, Neoplastic [MESH:D002471] (3389) |
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Reperfusion Injury [MESH:D015427] (4968) |
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Feminization [MESH:D005262] (655) |
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Obesity [MESH:D009765] (4454) |
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Seizures [MESH:D012640] (4502) |
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Muscular Atrophy [MESH:D009133] (1234) |
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Insulin-Like Growth Factor I Deficiency [MESH:C563867] (346) |
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Hyperalgesia [MESH:D006930] (3929) |
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C25. Chemically-Induced Disorders |
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C25. Chemically-Induced Disorders |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Drug-Induced Liver Injury [MESH:D056486] (4936) |
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Psychoses, Substance-Induced [MESH:D011605] (2053) |
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Amphetamine-Related Disorders [MESH:D019969] (2858) |
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Cocaine-Related Disorders [MESH:D019970] (3054) |
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Psychoses, Substance-Induced [MESH:D011605] (2052) |
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Liver Cirrhosis, Alcoholic [MESH:D008104] (3066) |
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D02. Organic Chemicals |
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D02. Organic Chemicals |
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Organophosphorus Compounds [MESH:D009943] (2593) |
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F. Psychiatry and Psychology |
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F. Psychiatry and Psychology |
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Amyotrophic Lateral Sclerosis 6, Autosomal Recessive [MESH:C567699] (54) |
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Aromatase deficiency [MESH:C537436] (277) |
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Lipoid congenital adrenal hyperplasia [MESH:C537027] (289) |
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