osteogenesis imperfecta type 10
osteogenesis imperfecta that has material basis in mutation in the SERPINH gene on chromosome 11q13
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osteogenesis imperfecta type 10
Summary
osteogenesis imperfecta type 10 is a rare disease[1].
Key Facts
- osteogenesis imperfecta type 10's instance of is recorded as rare disease[2].
- osteogenesis imperfecta type 10's instance of is recorded as class of disease[3].
- osteogenesis imperfecta type 10's subclass of is recorded as osteogenesis imperfecta[4].
- osteogenesis imperfecta type 10's subclass of is recorded as genetic disease[5].
- osteogenesis imperfecta type 10's OMIM ID is recorded as 613848[6].
- osteogenesis imperfecta type 10's Disease Ontology ID is recorded as DOID:0110346[7].
- osteogenesis imperfecta type 10's Orphanet ID is recorded as 216812[8].
- osteogenesis imperfecta type 10's health specialty is recorded as medical genetics[9].
- osteogenesis imperfecta type 10's genetic association is recorded as SERPINH1[10].
- osteogenesis imperfecta type 10's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110346[11].
- osteogenesis imperfecta type 10's exact match is recorded as http://identifiers.org/doid/DOID:0110346[12].
- osteogenesis imperfecta type 10's UMLS CUI is recorded as C3151211[13].
- osteogenesis imperfecta type 10's ICD-10-CM is recorded as Q78.0[14].
- osteogenesis imperfecta type 10's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- osteogenesis imperfecta type 10's Mondo ID is recorded as MONDO_0013459[16].
- osteogenesis imperfecta type 10's UniProt disease ID is recorded as DI-03068[17].