osteogenesis imperfecta type 15
osteogenesis imperfecta that has material basis in mutation in the WNT1 gene on chromosome 12q13
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osteogenesis imperfecta type 15
Summary
osteogenesis imperfecta type 15 is a rare disease[1].
Key Facts
- osteogenesis imperfecta type 15's instance of is recorded as rare disease[2].
- osteogenesis imperfecta type 15's instance of is recorded as class of disease[3].
- osteogenesis imperfecta type 15's subclass of is recorded as osteogenesis imperfecta[4].
- osteogenesis imperfecta type 15's subclass of is recorded as genetic disease[5].
- osteogenesis imperfecta type 15's OMIM ID is recorded as 615220[6].
- osteogenesis imperfecta type 15's Disease Ontology ID is recorded as DOID:0110347[7].
- osteogenesis imperfecta type 15's Orphanet ID is recorded as 216812[8].
- osteogenesis imperfecta type 15's Orphanet ID is recorded as 216820[9].
- osteogenesis imperfecta type 15's health specialty is recorded as medical genetics[10].
- osteogenesis imperfecta type 15's genetic association is recorded as WNT1[11].
- osteogenesis imperfecta type 15's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110347[12].
- osteogenesis imperfecta type 15's exact match is recorded as http://identifiers.org/doid/DOID:0110347[13].
- osteogenesis imperfecta type 15's UMLS CUI is recorded as C3808844[14].
- osteogenesis imperfecta type 15's ICD-10-CM is recorded as Q78.0[15].
- osteogenesis imperfecta type 15's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- osteogenesis imperfecta type 15's Mondo ID is recorded as MONDO_0014086[17].
- osteogenesis imperfecta type 15's UniProt disease ID is recorded as DI-03754[18].