osteogenesis imperfecta type 13
osteogenesis imperfecta that has material basis in mutation in the BMP1 gene on chromosome 8p21
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osteogenesis imperfecta type 13
Summary
osteogenesis imperfecta type 13 is a rare disease[1].
Key Facts
- osteogenesis imperfecta type 13's instance of is recorded as rare disease[2].
- osteogenesis imperfecta type 13's instance of is recorded as class of disease[3].
- osteogenesis imperfecta type 13's subclass of is recorded as osteogenesis imperfecta[4].
- osteogenesis imperfecta type 13's subclass of is recorded as genetic disease[5].
- osteogenesis imperfecta type 13's OMIM ID is recorded as 614856[6].
- osteogenesis imperfecta type 13's Disease Ontology ID is recorded as DOID:0110342[7].
- osteogenesis imperfecta type 13's Orphanet ID is recorded as 216812[8].
- osteogenesis imperfecta type 13's health specialty is recorded as medical genetics[9].
- osteogenesis imperfecta type 13's genetic association is recorded as BMP1[10].
- osteogenesis imperfecta type 13's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110342[11].
- osteogenesis imperfecta type 13's exact match is recorded as http://identifiers.org/doid/DOID:0110342[12].
- osteogenesis imperfecta type 13's UMLS CUI is recorded as C3553887[13].
- osteogenesis imperfecta type 13's ICD-10-CM is recorded as Q78.0[14].
- osteogenesis imperfecta type 13's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- osteogenesis imperfecta type 13's Mondo ID is recorded as MONDO_0013924[16].
- osteogenesis imperfecta type 13's UniProt disease ID is recorded as DI-03557[17].