Cataract, alopecia, oral mucosal disorder, and psoriasis-like syndrome

Preferred Label : Cataract, alopecia, oral mucosal disorder, and psoriasis-like syndrome;

Symbol : CAOP;

Type : Phenotype, molecular basis known;

Alternative titles and symbols : Caop syndrome;

Prefixed ID : #621252;

Details

Origin ID

621252;

Genes related to phenotype
- Membrane-bound transcription factor protease, site 1 [OMIM gene]

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