Keratoderma-ichthyosis-deafness syndrome, autosomal recessive

Preferred Label : Keratoderma-ichthyosis-deafness syndrome, autosomal recessive;

Symbol : KDIDAR;

Type : Phenotype, molecular basis known;

Prefixed ID : #620009;

Details

Origin ID

620009;

UMLS CUI

C5774200;

Genes related to phenotype
- Vps33b late endosome and lysosome associated [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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