Select any link to see items in a related category.

more general categories	information about this item
A. Anatomy	A. Anatomy
Body Regions [MESH:D001829] (867)
Extremities [MESH:D005121] (484)
Upper Extremity [MESH:D034941] (441)
Hand [MESH:D006225] (428)
Fingers [MESH:D005385] (422)	Syndactyly, type 3 [MESH:C538154] (192)
C04. Neoplasms	C04. Neoplasms
Neoplasms [MESH:D009369] (10293)
Neoplasms by Histologic Type [MESH:D009370] (8793)
Neoplasms, Glandular and Epithelial [MESH:D009375] (7760)	Adenoma [MESH:D000236] (4051)
Neoplasms by Site [MESH:D009371] (9169)	Skin Neoplasms [MESH:D012878] (2992)
Thoracic Neoplasms [MESH:D013899] (6032)
Respiratory Tract Neoplasms [MESH:D012142] (6020)	Lung Neoplasms [MESH:D008175] (6015)
Urogenital Neoplasms [MESH:D014565] (7002)
Genital Neoplasms, Male [MESH:D005834] (6224)	Prostatic Neoplasms [MESH:D011471] (6135)
C05. Musculoskeletal Diseases	C05. Musculoskeletal Diseases
Musculoskeletal Diseases [MESH:D009140] (8705)
Bone Diseases [MESH:D001847] (5801)
Bone Diseases, Developmental [MESH:D001848] (3315)
Dysostoses [MESH:D004413] (1019)
Craniofacial Dysostosis [MESH:D003394] (391)	Hallermann's Syndrome [MESH:D006210] (193)
Synostosis [MESH:D013580] (817)
Syndactyly [MESH:D013576] (487)	Syndactyly, type 3 [MESH:C538154] (192)
	Oculodentodigital Dysplasia [MESH:C563160] (192)
	Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)
Foot Deformities [MESH:D005530] (553)
Foot Deformities, Congenital [MESH:D005532] (538)	Oculodentodigital Dysplasia [MESH:C563160] (192)
Musculoskeletal Abnormalities [MESH:D009139] (3796)
Craniofacial Abnormalities [MESH:D019465] (3098)	Oculodentodigital Dysplasia [MESH:C563160] (192)
	Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)
Craniofacial Dysostosis [MESH:D003394] (391)	Hallermann's Syndrome [MESH:D006210] (193)
Limb Deformities, Congenital [MESH:D017880] (1813)
Lower Extremity Deformities, Congenital [MESH:D038061] (560)
Foot Deformities, Congenital [MESH:D005532] (538)	Oculodentodigital Dysplasia [MESH:C563160] (192)
Syndactyly [MESH:D013576] (487)	Syndactyly, type 3 [MESH:C538154] (192)
	Oculodentodigital Dysplasia [MESH:C563160] (192)
	Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)
Synostosis [MESH:D013580] (817)
Syndactyly [MESH:D013576] (487)	Syndactyly, type 3 [MESH:C538154] (192)
	Oculodentodigital Dysplasia [MESH:C563160] (192)
	Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)
C06. Digestive System Diseases	C06. Digestive System Diseases
Digestive System Diseases [MESH:D004066] (9461)
Liver Diseases [MESH:D008107] (8167)	Drug-Induced Liver Injury [MESH:D056486] (4936)
C07. Stomatognathic Diseases	C07. Stomatognathic Diseases
Stomatognathic Diseases [MESH:D009057] (5348)
Stomatognathic System Abnormalities [MESH:D018640] (1705)
Tooth Abnormalities [MESH:D014071] (622)	Oculodentodigital Dysplasia [MESH:C563160] (192)
	Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)
Tooth Diseases [MESH:D014076] (742)
Tooth Abnormalities [MESH:D014071] (622)	Oculodentodigital Dysplasia [MESH:C563160] (192)
	Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)
C08. Respiratory Tract Diseases	C08. Respiratory Tract Diseases
Respiratory Tract Diseases [MESH:D012140] (7881)
Lung Diseases [MESH:D008171] (7249)	Lung Neoplasms [MESH:D008175] (6012)
Respiratory Tract Neoplasms [MESH:D012142] (6053)	Lung Neoplasms [MESH:D008175] (6013)
C10. Nervous System Diseases	C10. Nervous System Diseases
Nervous System Diseases [MESH:D009422] (13325)
Neurodegenerative Diseases [MESH:D019636] (6613)
Heredodegenerative Disorders, Nervous System [MESH:D020271] (3243)
Amyloid Neuropathies, Familial [MESH:D028227] (137)	Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)
Neuromuscular Diseases [MESH:D009468] (7336)
Peripheral Nervous System Diseases [MESH:D010523] (6151)
Amyloid Neuropathies [MESH:D017772] (139)
Amyloid Neuropathies, Familial [MESH:D028227] (137)	Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)
Mononeuropathies [MESH:D020422] (604)
Median Neuropathy [MESH:D020423] (153)	Carpal Tunnel Syndrome [MESH:D002349] (147)
Nerve Compression Syndromes [MESH:D009408] (166)	Carpal Tunnel Syndrome [MESH:D002349] (147)
C11. Eye Diseases	C11. Eye Diseases
Eye Diseases [MESH:D005128] (6245)
Eye Abnormalities [MESH:D005124] (1233)	Oculodentodigital Dysplasia [MESH:C563160] (192)
	Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)
C12. Male Urogenital Diseases	C12. Male Urogenital Diseases
Male Urogenital Diseases [MESH:D052801] (8891)
Genital Diseases, Male [MESH:D005832] (6794)
Genital Neoplasms, Male [MESH:D005834] (6224)	Prostatic Neoplasms [MESH:D011471] (6135)
Prostatic Diseases [MESH:D011469] (6204)	Prostatic Neoplasms [MESH:D011471] (6135)
Urogenital Neoplasms [MESH:D014565] (6932)
Genital Neoplasms, Male [MESH:D005834] (6224)	Prostatic Neoplasms [MESH:D011471] (6135)
C14. Cardiovascular Diseases	C14. Cardiovascular Diseases
Cardiovascular Diseases [MESH:D002318] (10123)
Cardiovascular Abnormalities [MESH:D018376] (3153)
Heart Defects, Congenital [MESH:D006330] (2447)	Hypoplastic Left Heart Syndrome [MESH:D018636] (194)
Heart Diseases [MESH:D006331] (8614)	Arrhythmias, Cardiac [MESH:D001145] (4679)
Cardiomyopathies [MESH:D009202] (5331)	Myocardial Reperfusion Injury [MESH:D015428] (3500)
Heart Defects, Congenital [MESH:D006330] (2443)	Hypoplastic Left Heart Syndrome [MESH:D018636] (194)
Myocardial Ischemia [MESH:D017202] (5787)	Myocardial Reperfusion Injury [MESH:D015428] (3500)
Coronary Disease [MESH:D003327] (3439)	Coronary Aneurysm [MESH:D003323] (204)
Vascular Diseases [MESH:D014652] (8691)	Hypertension [MESH:D006973] (5655)
Aneurysm [MESH:D000783] (1886)	Coronary Aneurysm [MESH:D003323] (204)
Myocardial Ischemia [MESH:D017202] (5791)	Myocardial Reperfusion Injury [MESH:D015428] (3500)
Coronary Disease [MESH:D003327] (3439)	Coronary Aneurysm [MESH:D003323] (204)
Reperfusion Injury [MESH:D015427] (4968)	Myocardial Reperfusion Injury [MESH:D015428] (3500)
C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities	C16. Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] (12152)
Congenital Abnormalities [MESH:D000013] (8109)
Cardiovascular Abnormalities [MESH:D018376] (3294)
Heart Defects, Congenital [MESH:D006330] (2611)	Hypoplastic Left Heart Syndrome [MESH:D018636] (194)
Eye Abnormalities [MESH:D005124] (1233)	Oculodentodigital Dysplasia [MESH:C563160] (192)
	Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)
Musculoskeletal Abnormalities [MESH:D009139] (3779)
Craniofacial Abnormalities [MESH:D019465] (3064)	Oculodentodigital Dysplasia [MESH:C563160] (192)
	Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)
Craniofacial Dysostosis [MESH:D003394] (391)	Hallermann's Syndrome [MESH:D006210] (193)
Limb Deformities, Congenital [MESH:D017880] (1813)
Foot Deformities, Congenital [MESH:D005532] (538)	Oculodentodigital Dysplasia [MESH:C563160] (192)
Syndactyly [MESH:D013576] (487)	Syndactyly, type 3 [MESH:C538154] (192)
	Oculodentodigital Dysplasia [MESH:C563160] (192)
	Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)
Synostosis [MESH:D013580] (817)
Syndactyly [MESH:D013576] (487)	Syndactyly, type 3 [MESH:C538154] (192)
	Oculodentodigital Dysplasia [MESH:C563160] (192)
	Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)
Stomatognathic System Abnormalities [MESH:D018640] (1705)
Tooth Abnormalities [MESH:D014071] (622)	Oculodentodigital Dysplasia [MESH:C563160] (192)
	Oculodentodigital Dysplasia, Autosomal Recessive [MESH:C567605] (192)
Genetic Diseases, Inborn [MESH:D030342] (9766)
Heredodegenerative Disorders, Nervous System [MESH:D020271] (3465)
Amyloid Neuropathies, Familial [MESH:D028227] (137)	Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)
Metabolism, Inborn Errors [MESH:D008661] (6032)
Amyloidosis, Familial [MESH:D028226] (696)
Amyloid Neuropathies, Familial [MESH:D028227] (137)	Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)
C17. Skin and Connective Tissue Diseases	C17. Skin and Connective Tissue Diseases
Skin Diseases [MESH:D012871] (8774)	Skin Neoplasms [MESH:D012878] (2991)
Dermatitis [MESH:D003872] (4530)	Drug Eruptions [MESH:D003875] (2697)
C18. Nutritional and Metabolic Diseases	C18. Nutritional and Metabolic Diseases
Metabolic Diseases [MESH:D008659] (9025)
Metabolism, Inborn Errors [MESH:D008661] (6028)
Amyloidosis, Familial [MESH:D028226] (696)
Amyloid Neuropathies, Familial [MESH:D028227] (137)	Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)
Proteostasis Deficiencies [MESH:D057165] (3522)
Amyloidosis [MESH:D000686] (791)
Amyloid Neuropathies [MESH:D017772] (139)
Amyloid Neuropathies, Familial [MESH:D028227] (137)	Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)
Amyloidosis, Familial [MESH:D028226] (696)
Amyloid Neuropathies, Familial [MESH:D028227] (137)	Amyloidosis, Hereditary, Transthyretin-Related [MESH:C567782] (136)
C19. Endocrine System Diseases	C19. Endocrine System Diseases
Endocrine System Diseases [MESH:D004700] (8062)
Thyroid Diseases [MESH:D013959] (2808)
Hyperthyroxinemia [MESH:D006981] (659)	Dystransthyretinemic Euthyroidal Hyperthyroxinemia [MESH:C567719] (136)
C20. Immune System Diseases	C20. Immune System Diseases
Immune System Diseases [MESH:D007154] (7674)
Hypersensitivity [MESH:D006967] (5873)
Drug Hypersensitivity [MESH:D004342] (4000)	Drug Eruptions [MESH:D003875] (2695)
C23. Pathological Conditions, Signs and Symptoms	C23. Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical [MESH:D020763] (6074)
Hernia [MESH:D006547] (2825)	Hernia, Diaphragmatic [MESH:D006548] (2647)
Pathologic Processes [MESH:D010335] (9863)	Arrhythmias, Cardiac [MESH:D001145] (4658)
Postoperative Complications [MESH:D011183] (5311)
Reperfusion Injury [MESH:D015427] (4968)	Myocardial Reperfusion Injury [MESH:D015428] (3500)
C25. Chemically-Induced Disorders	C25. Chemically-Induced Disorders
Drug-Related Side Effects and Adverse Reactions [MESH:D064420] (5839)	Drug-Induced Liver Injury [MESH:D056486] (4936)
Drug Hypersensitivity [MESH:D004342] (4001)	Drug Eruptions [MESH:D003875] (2697)
Poisoning [MESH:D011041] (6703)	Drug-Induced Liver Injury [MESH:D056486] (4936)
C26. Wounds and Injuries	C26. Wounds and Injuries
Wounds and Injuries [MESH:D014947] (5171)
Sprains and Strains [MESH:D013180] (153)
Cumulative Trauma Disorders [MESH:D012090] (151)	Carpal Tunnel Syndrome [MESH:D002349] (147)
D02. Organic Chemicals	D02. Organic Chemicals
Organic Chemicals [MESH:D009930] (75987)	Nitriles [MESH:D009570] (810)