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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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