- OMIM ID
-
183300
- OMIM term:
- SPLENOGONADAL FUSION WITH LIMB DEFECTS AND MICROGNATHIA
- Alternative terms:
-
SPLENOGONADAL FUSION LIMB DEFECT SYNDROME
SGFLD SYNDROME
- (∗) Location:
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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