pachyonychia congenita
rare group of autosomal dominant skin disorders that are caused by a mutation in one of five different keratin genes
Press Enter · cited answer in seconds
0 sources
pachyonychia congenita
Summary
pachyonychia congenita is a rare disease[1]. It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[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 has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[2] It is known by 13 alternative names across languages and contexts.[17]