pachyonychia congenita
rare group of autosomal dominant skin disorders that are caused by a mutation in one of five different keratin genes
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pachyonychia congenita
Summary
pachyonychia congenita is a rare disease[1]. It draws 46 Wikipedia views per month (rare_disease category, ranking #218 of 627).[2]
Key Facts
- pachyonychia congenita's instance of is recorded as rare disease[3].
- pachyonychia congenita's instance of is recorded as syndrome[4].
- pachyonychia congenita's instance of is recorded as class of disease[5].
- pachyonychia congenita is a type of autosomal dominant disease[6].
- pachyonychia congenita is a type of ectodermal dysplasia[7].
- pachyonychia congenita is a type of nail disease[8].
- pachyonychia congenita is a type of skin disease[9].
- pachyonychia congenita's NCI Thesaurus ID is recorded as C84986[10].
- pachyonychia congenita's health specialty is recorded as medical genetics[11].
- pachyonychia congenita's genetic association is recorded as KRT16[12].
- pachyonychia congenita's genetic association is recorded as KRT17[13].
- pachyonychia congenita's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050449[14].
- pachyonychia congenita's exact match is recorded as http://identifiers.org/doid/DOID:0050449[15].
- pachyonychia congenita's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
pachyonychia congenita draws 46 Wikipedia views per month (rare_disease category, ranking #218 of 627).[2] It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[17] It is known by 13 alternative names across languages and contexts.[18]