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Disease Ontology Browser
chondrodysplasia punctata (DOID:2581)
Alliance: disease page
Synonyms: Chondrodysplasia punctata congenita
Alt IDs: OMIM:215105, ICD10CM:Q77.3, MESH:D002806, NCI:C84632, ORDO:93442, UMLS_CUI:C0008445
Definition: A syndrome that is characterized by abnormal calcification of the epiphyses, causing stippling in radiography.

Disease References using Mouse Models (6)
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory