Intellectual developmental disorder, X-linked 110

Preferred Label : Intellectual developmental disorder, X-linked 110;

Symbol : XLID110;

Type : Phenotype, molecular basis known;

Prefixed ID : #301095;

Détails

Origin ID

301095;

UMLS CUI

C5774180;

Genes related to phenotype
- Fibroblast growth factor 13 [OMIM gene]
Semantic type(s)
- Mental or Behavioral Dysfunction [UMLS semantic type]

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