All diseases

OMIM ID
119100
OMIM term:
SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY 1; SHFLD1
Alternative terms:
SPLIT-HAND/FOOT MALFORMATION WITH LONG BONE DEFICIENCY; SHFLD
CLEFT HAND AND ABSENT TIBIA
APLASIA OF TIBIA WITH ECTRODACTYLY
TIBIAL APLASIA WITH SPLIT-HAND/SPLIT-FOOT DEFORMITY
ECTRODACTYLY WITH APLASIA OF LONG BONES
(∗) Location:
1q42.2-q43  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/u0pegyw6