Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2

Preferred Label : Cataracts, hearing impairment, nephrotic syndrome, and enterocolitis 2;

Symbol : CHINE2;

Type : Phenotype, molecular basis known;

Prefixed ID : #620425;

Details

Origin ID

620425;

UMLS CUI

C5830590;

Genes related to phenotype
- Nop10 ribonucleoprotein [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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