All diseases

OMIM ID
268310
OMIM term:
ROBINOW SYNDROME, AUTOSOMAL RECESSIVE; RRS
Alternative terms:
COSTOVERTEBRAL SEGMENTATION DEFECT WITH MESOMELIA, FORMERLY
COVESDEM SYNDROME, FORMERLY ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH APLASIA/HYPOPLASIA OF PHALANGES AND METACARPALS/METATARSALS, INCLUDED
ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, WITH BRACHY-SYN-POLYDACTYLY, INCLUDED
(∗) Location:
9q22.31  
(†) Associated OMIM genes:
ROR2  
(‡) Associated MGI genes:
Ror2  

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