All diseases

OMIM ID
601559
OMIM term:
STUVE-WIEDEMANN SYNDROME
Alternative terms:
STWS; SWS
SCHWARTZ-JAMPEL SYNDROME, TYPE 2; SJS2
SCHWARTZ-JAMPEL SYNDROME, NEONATAL
STUVE-WIEDEMANN/SCHWARTZ-JAMPEL TYPE 2 SYNDROME
(∗) Location:
5p13.1  
(†) Associated OMIM genes:
LIFR  
(‡) Associated MGI genes:

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