All diseases

OMIM ID
600145
OMIM term:
SACRAL DEFECT WITH ANTERIOR MENINGOCELE
Alternative terms:
SDAM CAUDAL DYSGENESIS SYNDROME, INCLUDED
CAUDAL REGRESSION SYNDROME, INCLUDED
SACRAL AGENESIS, INCLUDED
SIRENOMELIA, INCLUDED
(∗) Location:
1p13.1  
(†) Associated OMIM genes:
VANGL1  
(‡) Associated MGI genes:

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