Orphanet: MORM syndrome
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MORM syndrome

Disease definition

A rare genetic syndromic intellectual disability characterized by language delay and mild to moderate intellectual disability associated with truncal obesity, congenital nonprogressive retinal dystrophy with poor night vision and reduced visual acuity, and micropenis in males. Cataracts may occur in the second or third decade of life.

ORPHA:75858

Classification level: Disorder
  • Synonym(s):
    • Intellectual disability-truncal obesity-retinal dystrophy-micropenis syndrome
  • Prevalence: Unknown
  • Inheritance: Autosomal recessive 
  • Age of onset: -
  • ICD-10: -
  • OMIM: 610156
  • UMLS: C1857802
  • MeSH: C536984
  • GARD: 10121
  • MedDRA: -
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