All diseases

OMIM ID
135750
OMIM term:
LAURIN-SANDROW SYNDROME
Alternative terms:
LSS
SANDROW SYNDROME
MIRROR HANDS AND FEET WITH NASAL DEFECTS
TETRAMELIC MIRROR-IMAGE POLYDACTYLY; TMIP
MIRROR-IMAGE POLYDACTYLY; MIP
FIBULA AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUS LAURIN-SANDROW SYNDROME, SEGMENTAL, INCLUDED
(∗) Location:
14q13   14q13.3-q21.1  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/stcs8b1y