All diseases

OMIM ID
249420
OMIM term:
FRANK-TER HAAR SYNDROME; FTHS
Alternative terms:
TER HAAR SYNDROME
MELNICK-NEEDLES SYNDROME, AUTOSOMAL RECESSIVE, FORMERLY
(∗) Location:
5q35.1  
(†) Associated OMIM genes:
SH3PXD2B  
(‡) Associated MGI genes:
Sh3pxd2b  

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* quick link - http://q.sanger.ac.uk/64jj5yec