Search Ontology:
Human Disease

Robinow syndrome

Term ID
DOID:0060254
Synonyms
  • acral dysostosis with facial and genital abnormalities
  • fetal face syndrome
  • Robinow dwarfism
Definition
A syndrome characterized by mild to moderate short stature due to growth delays after birth, distinctive craniofacial abnormalities, skeletal malformations and genital abnormalities. (3)
References
  • GARD:312
  • ICD10CM:Q87.19
  • MESH:C562492
  • MIM:PS268310
  • NCI:C85048
  • ORDO:97360
  • SNOMEDCT_US_2023_03_01:76520005
  • UMLS_CUI:C0265205
Ontology
Human Disease   ( DOID:0060254 )
Relationships
is a type of
has subtype
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Genes Involved
Zebrafish Models