Related MeSH Hierarchy (6)
Diseases [C] » Nervous System Diseases [C10] » Neurocutaneous Syndromes
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Abnormalities, Multiple » Ectodermal Dysplasia » Neurocutaneous Syndromes
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Congenital Abnormalities » Skin Abnormalities » Ectodermal Dysplasia » Neurocutaneous Syndromes
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Skin Diseases, Genetic » Ectodermal Dysplasia » Neurocutaneous Syndromes
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Abnormalities » Ectodermal Dysplasia » Neurocutaneous Syndromes
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Ectodermal Dysplasia » Neurocutaneous Syndromes
Description
A group of disorders characterized by ectodermal-based malformations and neoplastic growths in the skin, nervous system, and other organs. MeSH
Hierarchy View
Subtype Terms (6)
Ataxia Telangiectasia
28 drugs (25 approved, 3 experimental)
Neurofibromatoses
16 drugs (14 approved, 2 experimental)
Sturge-Weber Syndrome
5 drugs (4 approved, 1 experimental)
Tuberous Sclerosis
13 drugs (10 approved, 3 experimental)
von Hippel-Lindau Disease
18 drugs (13 approved, 5 experimental)
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UMLS Data
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