Diabetes, deafness, developmental delay, and short stature syndrome

Preferred Label : Diabetes, deafness, developmental delay, and short stature syndrome;

Symbol : DDDS;

Type : Phenotype, molecular basis known;

Prefixed ID : #620651;

Details

Origin ID

620651;

UMLS CUI

C5882732;

Genes related to phenotype
- Mesencephalic astrocyte-derived neurotrophic factor [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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