brachydactyly type C
), have been reported in BDC patients. Many studies support an autosomal dominant mode of inheritance.
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brachydactyly type C
Summary
brachydactyly type C is a developmental defect during embryogenesis[1].
Key Facts
- brachydactyly type C's instance of is recorded as developmental defect during embryogenesis[2].
- brachydactyly type C's instance of is recorded as genetic disease[3].
- brachydactyly type C's instance of is recorded as rare disease[4].
- brachydactyly type C's instance of is recorded as class of disease[5].
- brachydactyly type C is a type of brachydactyly[6].
- brachydactyly type C is a type of syndrome with brachydactyly[7].
- brachydactyly type C is a type of autosomal dominant disease[8].
- brachydactyly type C's health specialty is recorded as medical genetics[9].
- brachydactyly type C's genetic association is recorded as GDF5[10].
- brachydactyly type C's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110970[11].
- brachydactyly type C's exact match is recorded as http://identifiers.org/doid/DOID:0110970[12].
- brachydactyly type C's exact match is recorded as http://purl.obolibrary.org/obo/HP_0009373[13].
- brachydactyly type C's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_93384[14].
- brachydactyly type C's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].