Intellectual developmental disorder, X-linked, syndromic 37

Preferred Label : Intellectual developmental disorder, X-linked, syndromic 37;

Symbol : MRXS37;

Type : Phenotype, molecular basis known;

Prefixed ID : #301118;

Détails

Origin ID

301118;

UMLS CUI

C5935567;

Genes related to phenotype
- Zinc finger protein, X-linked [OMIM gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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