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DO Term : rhizomelic chondrodysplasia punctata [DOID:2580] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  A chondrodysplasia punctata that is characterized by disproportionately short stature primarily affecting the proximal parts of the extremities, a typical facial appearance including a broad nasal bridge, epicanthus, high-arched palate, dysplastic external ears, and micrognathia, congenital contractures, characteristic ocular involvement, dwarfism, and severe mental retardation with spasticity.
  • synonyms:
  • Chondrodysplasia Punctata, Rhizomelic Form,
  • ORDO:177,
  • GARD:13160,
  • ICD10CM:E71.540,
  • SNOMEDCT_US_2023_03_01:56692003,
  • OMIM:PS215100,
  • MESH:D018902,
  • UMLS_CUI:C0282529,
  • NCI:C85047,
  • PS215100
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