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Metadata
ID DOID:2580
Name rhizomelic chondrodysplasia punctata
Definition 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.
http://en.wikipedia.org/wiki/Rhizomelic_chondrodysplasia_punctata, http://ghr.nlm.nih.gov/condition/rhizomelic-chondrodysplasia-punctata, https://www.ncbi.nlm.nih.gov/pubmed/15679822
Xrefs

GARD:13160

ICD10CM:E71.540

MESH:D018902

NCI:C85047

OMIM:PS215100

ORDO:177

SNOMEDCT_US_2023_03_01:56692003

UMLS_CUI:C0282529

Subsets

DO_rare_slim

NCIthesaurus

Synonyms

Chondrodysplasia Punctata, Rhizomelic Form [EXACT]

Parent Relationships

is_a chondrodysplasia punctata

is_a autosomal recessive disease

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