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DO Term : MEHMO syndrome [DOID:0060801] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A syndromic X-linked intellectual disability characterized by severe intellectual deficit, epilepsy, microcephaly, hypogenitalism and obesity with variable occurrence of growth delay and diabetes that has_material_basis_in hemizygous mutation in the EIF2S3 gene on chromosome Xp22.
  • synonyms:
  • SNOMEDCT_US_2023_03_01:722037004,
  • OMIM:300148,
  • mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity,
  • MRXS25,
  • syndromic X-linked mental retardation 25,
  • 300148,
  • MRXS20,
  • X-linked intellectual disability-epileptic seizures-hypogenitalism-microcephaly-obesity syndrome,
  • syndromic X-linked mental retardation 20,
  • ORDO:85282,
  • MESH:C537451,
  • UMLS_CUI:C1846278
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Disease

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Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents