Pituitary hormone deficiency, combined or isolated, 8

Preferred Label : Pituitary hormone deficiency, combined or isolated, 8;

Symbol : CPHD8;

Type : Phenotype, molecular basis known;

Prefixed ID : #620303;

Details

Origin ID

620303;

UMLS CUI

C5830375;

Genes related to phenotype
- Roundabout guidance receptor 1 [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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