brachydactyly type A1D
brachydactyly type A1 that has material basis in heterozygous mutation in the BMPR1B gene on chromosome 4q22
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brachydactyly type A1D
Summary
brachydactyly type A1D is a developmental defect during embryogenesis[1].
Key Facts
- brachydactyly type A1D's instance of is recorded as developmental defect during embryogenesis[2].
- brachydactyly type A1D's instance of is recorded as rare disease[3].
- brachydactyly type A1D's instance of is recorded as class of disease[4].
- brachydactyly type A1D's subclass of is recorded as brachydactyly type A1[5].
- brachydactyly type A1D's OMIM ID is recorded as 616849[6].
- brachydactyly type A1D's Disease Ontology ID is recorded as DOID:0110978[7].
- brachydactyly type A1D's genetic association is recorded as BMPR1B[8].
- brachydactyly type A1D's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110978[9].
- brachydactyly type A1D's exact match is recorded as http://identifiers.org/doid/DOID:0110978[10].
- brachydactyly type A1D's UMLS CUI is recorded as C4225183[11].
- brachydactyly type A1D's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- brachydactyly type A1D's Mondo ID is recorded as MONDO_0014798[13].
- brachydactyly type A1D's UniProt disease ID is recorded as DI-04670[14].