A rare developmental defect during embryogenesis characterized by growth delay and multiorgan manifestations.

Synonyms:

Mulibrey growth disorder

MUL

Muscle-liver-brain-eye nanism

This is just here as a test because I lose it

Term information

database cross reference
expertlink
  • https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2576
hasDbXref
  • ICD-10:Q87.1
  • MeSH:D050336
  • OMIM:253250
  • UMLS:C2931895
  • UMLS:C0524582
  • MeSH:C538604
has age of onset
  • http://www.orpha.net/ORDO/Orphanet_409946
  • http://www.orpha.net/ORDO/Orphanet_409945
  • http://www.orpha.net/ORDO/Orphanet_409944
has annual incidence range
  • http://www.orpha.net/ORDO/Orphanet_409977
has inheritance
  • http://www.orpha.net/ORDO/Orphanet_409930
has point prevalence range
  • http://www.orpha.net/ORDO/Orphanet_409981
notation
  • ORPHA:2576
part of
  • http://www.orpha.net/ORDO/Orphanet_183570
  • http://www.orpha.net/ORDO/Orphanet_139021
present in
  • http://www.orpha.net/ORDO/Orphanet_409991
  • http://www.orpha.net/ORDO/Orphanet_410065