All diseases

OMIM ID
276820
OMIM term:
ULNA AND FIBULA, ABSENCE OF, WITH SEVERE LIMB DEFICIENCY
Alternative terms:
LIMB/PELVIS-HYPOPLASIA/APLASIA SYNDROME; LPHAS
AL-AWADI/RAAS-ROTHSCHILD SYNDROME; AARRS
SCHINZEL PHOCOMELIA SYNDROME
(∗) Location:
3p25.1  
(†) Associated OMIM genes:
WNT7A  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/ilo79694