Search Ontology:
Human Disease

chondrodysplasia punctata

Term ID
DOID:2581
Synonyms
  • Chondrodysplasia punctata congenita
Definition
A syndrome that is characterized by abnormal calcification of the epiphyses, causing stippling in radiography. (2)
References
  • GARD:8542
  • ICD10CM:Q77.3
  • MESH:D002806
  • MIM:215105
  • NCI:C84632
  • ORDO:93442
  • SNOMEDCT_US_2023_03_01:205486004
  • UMLS_CUI:C0008445
Ontology
Human Disease   ( DOID:2581 )
Relationships
is a type of
has subtype
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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