more general categories |
information about this item |
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4. Semantic Terms |
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4. Semantic Terms |
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Pharmacologic Substance [STY:T121] (11019) |
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Organic Chemical [STY:T109] (44144) |
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A. Anatomy |
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A. Anatomy |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Alveolar capillary dysplasia [MESH:C536590] (56) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Single upper central incisor [MESH:C537342] (50) |
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C02. Virus Diseases |
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C02. Virus Diseases |
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Burkitt Lymphoma [MESH:D002051] (691) |
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HIV Infections [MESH:D015658] (3402) |
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HIV Infections [MESH:D015658] (3296) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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C04. Neoplasms |
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C04. Neoplasms |
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Basal Cell Nevus Syndrome [MESH:D001478] (67) |
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Leukemia, Myeloid, Acute [MESH:D015470] (2176) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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Mastocytosis [MESH:D008415] (792) |
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Rhabdomyosarcoma [MESH:D012208] (789) |
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Rhabdomyosarcoma [MESH:D012208] (789) |
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Medulloblastoma [MESH:D008527] (1282) |
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Medulloblastoma [MESH:D008527] (1282) |
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Adenocarcinoma [MESH:D000230] (6565) |
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Basal Cell Nevus Syndrome [MESH:D001478] (67) |
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Basal Cell Nevus Syndrome [MESH:D001478] (67) |
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Medulloblastoma [MESH:D008527] (1282) |
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Medulloblastoma [MESH:D008527] (1282) |
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Meningioma [MESH:D008579] (978) |
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Medulloblastoma [MESH:D008527] (1282) |
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Medulloblastoma [MESH:D008527] (1282) |
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Meningioma [MESH:D008579] (978) |
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Skin Neoplasms [MESH:D012878] (2992) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Brain Neoplasms [MESH:D001932] (2764) |
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Meningioma [MESH:D008579] (978) |
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Lung Neoplasms [MESH:D008175] (6015) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Mammary Neoplasms, Experimental [MESH:D008325] (3268) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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Basal Cell Nevus Syndrome [MESH:D001478] (67) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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C05. Musculoskeletal Diseases |
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C05. Musculoskeletal Diseases |
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Basal Cell Nevus Syndrome [MESH:D001478] (67) |
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Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress [MESH:C567034] (27) |
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Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress [MESH:C567034] (27) |
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Cleft Palate [MESH:D002972] (1330) |
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Basal Cell Nevus Syndrome [MESH:D001478] (67) |
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Muscular Dystrophy, Limb-Girdle, Type 2G [MESH:C566599] (13) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 7 [MESH:C563660] (46) |
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Holoprosencephaly 3 [MESH:C564181] (50) |
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Cleft Palate [MESH:D002972] (1330) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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C06. Digestive System Diseases |
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C06. Digestive System Diseases |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Colonic Neoplasms [MESH:D003110] (4405) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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C07. Stomatognathic Diseases |
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C07. Stomatognathic Diseases |
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Cleft Palate [MESH:D002972] (1330) |
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Basal Cell Nevus Syndrome [MESH:D001478] (67) |
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Cleft Lip [MESH:D002971] (914) |
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Cleft Lip [MESH:D002971] (914) |
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Cleft Palate [MESH:D002972] (1330) |
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Macrostomia [MESH:D008265] (38) |
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Cleft Palate [MESH:D002972] (1330) |
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Cleft Lip [MESH:D002971] (914) |
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Cleft Palate [MESH:D002972] (1330) |
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Macrostomia [MESH:D008265] (38) |
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Single upper central incisor [MESH:C537342] (50) |
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Single upper central incisor [MESH:C537342] (50) |
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C08. Respiratory Tract Diseases |
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C08. Respiratory Tract Diseases |
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Asthma [MESH:D001249] (4098) |
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Lung Neoplasms [MESH:D008175] (6012) |
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Alveolar capillary dysplasia [MESH:C536590] (56) |
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Asthma [MESH:D001249] (3903) |
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Acute Lung Injury [MESH:D055371] (1907) |
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Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress [MESH:C567034] (27) |
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Rhinitis [MESH:D012220] (1134) |
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Congenital central hypoventilation syndrome [MESH:C536209] (341) |
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Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress [MESH:C567034] (27) |
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Congenital central hypoventilation syndrome [MESH:C536209] (341) |
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Asthma [MESH:D001249] (4098) |
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Rhinitis [MESH:D012220] (766) |
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Lung Neoplasms [MESH:D008175] (6013) |
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C09. Otorhinolaryngologic Diseases |
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C09. Otorhinolaryngologic Diseases |
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Rhinitis [MESH:D012220] (1134) |
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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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Brain Neoplasms [MESH:D001932] (2764) |
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Parkinson Disease, Secondary [MESH:D010302] (327) |
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Seizures [MESH:D012640] (4502) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress [MESH:C567034] (27) |
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Parkinson Disease, Secondary [MESH:D010302] (327) |
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Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 7 [MESH:C563660] (46) |
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Holoprosencephaly 3 [MESH:C564181] (50) |
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Brain Neoplasms [MESH:D001932] (2764) |
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Meningioma [MESH:D008579] (978) |
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Pain [MESH:D010146] (3875) |
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Seizures [MESH:D012640] (4514) |
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Catalepsy [MESH:D002375] (1429) |
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Tremor [MESH:D014202] (840) |
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Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress [MESH:C567034] (27) |
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Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress [MESH:C567034] (27) |
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Learning Disorders [MESH:D007859] (2727) |
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Stupor [MESH:D053608] (103) |
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Coma, Post-Head Injury [MESH:D020207] (55) |
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Amnesia [MESH:D000647] (1911) |
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Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18) |
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Pierson syndrome [MESH:C537185] (33) |
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Peripheral Nervous System Diseases [MESH:D010523] (6151) |
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Muscular Dystrophy, Limb-Girdle, Type 2G [MESH:C566599] (13) |
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Narcolepsy [MESH:D009290] (478) |
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Congenital central hypoventilation syndrome [MESH:C536209] (341) |
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Coma, Post-Head Injury [MESH:D020207] (55) |
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C11. Eye Diseases |
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C11. Eye Diseases |
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Pierson syndrome [MESH:C537185] (33) |
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Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50) |
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Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50) |
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Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18) |
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Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18) |
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Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18) |
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Pierson syndrome [MESH:C537185] (33) |
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Diabetic Retinopathy [MESH:D003930] (1371) |
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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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Prostatic Neoplasms [MESH:D011471] (6135) |
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Prostatic Neoplasms [MESH:D011471] (6135) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Pierson syndrome [MESH:C537185] (33) |
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Mesangial sclerosis, diffuse [MESH:C537346] (33) |
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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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Endometriosis [MESH:D004715] (2461) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Pierson syndrome [MESH:C537185] (33) |
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Mesangial sclerosis, diffuse [MESH:C537346] (33) |
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Urinary Bladder Neoplasms [MESH:D001749] (4079) |
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Prenatal Injuries [MESH:D049188] (1314) |
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C14. Cardiovascular Diseases |
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C14. Cardiovascular Diseases |
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Myocardial Ischemia [MESH:D017202] (5787) |
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Bradycardia [MESH:D001919] (1899) |
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Tachycardia [MESH:D013610] (3339) |
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Cardiomyopathy, Dilated, 1N [MESH:C564388] (13) |
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Cardiomyopathy, Dilated, 1AA [MESH:C567407] (27) |
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Cardiomyopathy, Dilated, 1N [MESH:C564388] (13) |
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Cardiomyopathy, Dilated, 1AA [MESH:C567407] (27) |
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Hypertension [MESH:D006973] (5655) |
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Myocardial Ischemia [MESH:D017202] (5791) |
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Reperfusion Injury [MESH:D015427] (4968) |
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Diabetic Retinopathy [MESH:D003930] (1371) |
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C15. Hemic and Lymphatic Diseases |
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C15. Hemic and Lymphatic Diseases |
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Burkitt Lymphoma [MESH:D002051] (691) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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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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Abnormalities, Drug-Induced [MESH:D000014] (1024) |
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Pierson syndrome [MESH:C537185] (33) |
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Basal Cell Nevus Syndrome [MESH:D001478] (67) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 7 [MESH:C563660] (46) |
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Holoprosencephaly 3 [MESH:C564181] (50) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 7 [MESH:C563660] (46) |
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Holoprosencephaly 3 [MESH:C564181] (50) |
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Pierson syndrome [MESH:C537185] (33) |
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Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50) |
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Microphthalmia, Isolated, with Coloboma 5 [MESH:C566899] (50) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 7 [MESH:C563660] (46) |
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Holoprosencephaly 3 [MESH:C564181] (50) |
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Cleft Palate [MESH:D002972] (1330) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 7 [MESH:C563660] (46) |
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Holoprosencephaly 3 [MESH:C564181] (50) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 7 [MESH:C563660] (46) |
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Holoprosencephaly 3 [MESH:C564181] (50) |
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Cleft Palate [MESH:D002972] (1330) |
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Cleft Lip [MESH:D002971] (914) |
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Cleft Palate [MESH:D002972] (1330) |
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Macrostomia [MESH:D008265] (38) |
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Single upper central incisor [MESH:C537342] (50) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Holoprosencephaly 7 [MESH:C563660] (46) |
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Holoprosencephaly 3 [MESH:C564181] (50) |
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Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress [MESH:C567034] (27) |
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Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18) |
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Muscular Dystrophy, Limb-Girdle, Type 2G [MESH:C566599] (13) |
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Basal Cell Nevus Syndrome [MESH:D001478] (67) |
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Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress [MESH:C567034] (27) |
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Alveolar capillary dysplasia [MESH:C536590] (56) |
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C17. Skin and Connective Tissue Diseases |
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C17. Skin and Connective Tissue Diseases |
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Mastocytosis [MESH:D008415] (60) |
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Skin Neoplasms [MESH:D012878] (2991) |
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Urticaria [MESH:D014581] (2668) |
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C19. Endocrine System Diseases |
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C19. Endocrine System Diseases |
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Diabetic Retinopathy [MESH:D003930] (1371) |
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Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress [MESH:C567034] (27) |
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Pancreatic Neoplasms [MESH:D010190] (3820) |
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Holoprosencephaly 9 [MESH:C563659] (35) |
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Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress [MESH:C567034] (27) |
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C20. Immune System Diseases |
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C20. Immune System Diseases |
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Drug Hypersensitivity [MESH:D004342] (4000) |
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Urticaria [MESH:D014581] (2668) |
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Asthma [MESH:D001249] (3914) |
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HIV Infections [MESH:D015658] (3402) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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Burkitt Lymphoma [MESH:D002051] (691) |
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C22. Animal Diseases |
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C22. Animal Diseases |
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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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Hernia, Diaphragmatic [MESH:D006548] (2647) |
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Bradycardia [MESH:D001919] (1899) |
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Tachycardia [MESH:D013610] (3339) |
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Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18) |
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Reperfusion Injury [MESH:D015427] (4968) |
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Mesangial sclerosis, diffuse [MESH:C537346] (33) |
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Edema [MESH:D004487] (3726) |
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Pain [MESH:D010146] (4511) |
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Hypothermia [MESH:D007035] (2075) |
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Pain [MESH:D010146] (3869) |
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Seizures [MESH:D012640] (4502) |
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Catalepsy [MESH:D002375] (1429) |
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Tremor [MESH:D014202] (840) |
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Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress [MESH:C567034] (27) |
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Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress [MESH:C567034] (27) |
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Learning Disorders [MESH:D007859] (2727) |
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Stupor [MESH:D053608] (103) |
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Amnesia [MESH:D000647] (1911) |
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Fibrosis Of Extraocular Muscles, Congenital, 2 [MESH:C566587] (18) |
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Pierson syndrome [MESH:C537185] (33) |
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Congenital central hypoventilation syndrome [MESH:C536209] (341) |
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C25. Chemically-Induced Disorders |
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C25. Chemically-Induced Disorders |
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Drug Hypersensitivity [MESH:D004342] (4001) |
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Amphetamine-Related Disorders [MESH:D019969] (2858) |
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Cocaine-Related Disorders [MESH:D019970] (3054) |
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C26. Wounds and Injuries |
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C26. Wounds and Injuries |
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Coma, Post-Head Injury [MESH:D020207] (55) |
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Coma, Post-Head Injury [MESH:D020207] (55) |
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D03. Heterocyclic Compounds |
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D03. Heterocyclic Compounds |
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Veratrum Alkaloids [MESH:D014704] (46) |
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