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PedAM

Pediatric Disease Annotations & Medicines




Disease alopecia
Phenotype C0020678|hypotrichosis
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PubMedID- 24052723 Hidrotic ectodermal dysplasia type 2 (hed2) or clouston syndrome (omim #129500) is a rare autosomal dominant genetic disorder which affects skin and its derivatives, characterized by the major triad of features: nail dystrophy, generalized hypotrichosis with alopecia and palmoplantar hyperkeratosis, frequently accompanied by normal perspiration and dentition.

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