osteogenesis imperfecta type 16
osteogenesis imperfecta that has material basis in contiguous gene deletion on chromosome 11p11
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osteogenesis imperfecta type 16
Summary
osteogenesis imperfecta type 16 is a class of disease[1].
Key Facts
- osteogenesis imperfecta type 16's instance of is recorded as class of disease[2].
- osteogenesis imperfecta type 16's subclass of is recorded as osteogenesis imperfecta[3].
- osteogenesis imperfecta type 16's OMIM ID is recorded as 616229[4].
- osteogenesis imperfecta type 16's Disease Ontology ID is recorded as DOID:0110345[5].
- osteogenesis imperfecta type 16's Orphanet ID is recorded as 216812[6].
- osteogenesis imperfecta type 16's health specialty is recorded as medical genetics[7].
- osteogenesis imperfecta type 16's genetic association is recorded as CREB3L1[8].
- osteogenesis imperfecta type 16's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110345[9].
- osteogenesis imperfecta type 16's exact match is recorded as http://identifiers.org/doid/DOID:0110345[10].
- osteogenesis imperfecta type 16's UMLS CUI is recorded as C4015610[11].
- osteogenesis imperfecta type 16's ICD-10-CM is recorded as Q78.0[12].
- osteogenesis imperfecta type 16's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- osteogenesis imperfecta type 16's Mondo ID is recorded as MONDO_0014544[14].
- osteogenesis imperfecta type 16's UniProt disease ID is recorded as DI-04377[15].