MEHMO syndrome

Summary
Synonym
  • MRXS20
  • MRXS25
  • X-linked intellectual disability-epileptic seizures-hypogenitalism-microcephaly-obesity syndrome
  • mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity
  • syndromic X-linked mental retardation 20
  • syndromic X-linked mental retardation 25
Definition
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 variation in the chromosome region Xp22.13-p21.1.
Super Class
X-linked recessive disease syndromic X-linked intellectual disability
Disease Ontology
DOID:0060801
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1968 EIF2S3 eukaryotic translation initiation factor 2 subunit gamma
Displaying 1 entry
Gene ID Gene Symbol Description Source
26905 Eif2s3x eukaryotic translation initiation factor 2, subunit 3, structural gene X-linked
The Human Phenotype Ontology
Displaying entries 1 - 10 of 59 in total
HPO ID HPO Term
HP:0000713 Agitation
HP:0001513 Obesity
HP:0000293 Full cheeks
HP:0001252 Hypotonia
HP:0000054 Micropenis
HP:0001347 Hyperreflexia
HP:0000340 Sloping forehead
HP:0002353 EEG abnormality
HP:0001182 Tapered finger
HP:0000028 Cryptorchidism
Displaying 1 entry
Gene ID Gene Symbol Description
1968 EIF2S3 eukaryotic translation initiation factor 2 subunit gamma

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Last updated: December 9, 2024