X-linked chondrodysplasia punctata
Human disease
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Summary
X-linked chondrodysplasia punctata is a class of disease[1].
Key Facts
- X-linked chondrodysplasia punctata's instance of is recorded as class of disease[2].
- X-linked chondrodysplasia punctata's subclass of is recorded as chondrodysplasia punctata[3].
- X-linked chondrodysplasia punctata's subclass of is recorded as X-linked recessive disease[4].
- X-linked chondrodysplasia punctata's MeSH descriptor ID is recorded as C002806[5].
- X-linked chondrodysplasia punctata's OMIM ID is recorded as 302950[6].
- X-linked chondrodysplasia punctata's Disease Ontology ID is recorded as DOID:0060292[7].
- X-linked chondrodysplasia punctata's Orphanet ID is recorded as 35173[8].
- X-linked chondrodysplasia punctata's health specialty is recorded as medical genetics[9].
- X-linked chondrodysplasia punctata's genetic association is recorded as EBP[10].
- X-linked chondrodysplasia punctata's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060292[11].
- X-linked chondrodysplasia punctata's exact match is recorded as http://identifiers.org/doid/DOID:0060292[12].
- X-linked chondrodysplasia punctata's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_35173[13].
- X-linked chondrodysplasia punctata's ICD-10-CM is recorded as Uruguay.3[14].
- X-linked chondrodysplasia punctata's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].