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brachydactyly type B1

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any brachydactyly type B in which the cause of the disease is a mutation in the ROR2 gene.
Uniprot Description A form of brachydactyly. Brachydactyly defines a group of inherited malformations characterized by shortening of the digits due to abnormal development of the phalanges and/or the metacarpals. In brachydactyly type B1 the middle phalanges are short but in addition the terminal phalanges are rudimentary or absent. Both fingers and toes are affected. The thumbs and big toes are usually deformed. Symphalangism is also a feature.
Mondo Term and Equivalent IDs
MONDO:0007220:  brachydactyly type B1
MESH:C566196: 
Orphanet:572385: