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MEHMO syndrome

Disease Export to PDF
Name:
MEHMO syndrome
Description:
A rare X-linked syndromic intellectual disability characterized by mild to profound intellectual disability, microcephaly, growth delay, and hypogenitalism. Obesity, early-onset diabetes and epilepsy are more variably present.
ORPHAcode:
85282
Synonyms:
X-linked intellectual disability-epileptic seizures-hypogenitalism-microcephaly-obesity syndrome
XREF(s):
Orphanet
OMIM
MeSH
ICD-10
Analyte(s):
EIF2S3
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14