Epidermolytic hyperkeratosis 2b, autosomal recessive

Preferred Label : Epidermolytic hyperkeratosis 2b, autosomal recessive;

Symbol : EHK2B;

Type : Phenotype, molecular basis known;

Prefixed ID : #620707;

Details

Origin ID

620707;

UMLS CUI

C5882753;

Genes related to phenotype
- Keratin 10, type I [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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