mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly and obesity syndrome

Preferred Label : mental retardation, epileptic seizures, hypogonadism and -genitalism, microcephaly and obesity syndrome;

Obsolete resource : true;

Approved symbol HGNC : MEHMO;

Chromosome HGNC : Xp22.13-p21.1;

Locus type HGNC : phenotype;

Détails

Origin ID

HGNC:6999;

UMLS CUI

C1417105;

Automatic exact mappings (from CISMeF team)
- Mehmo syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]

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