All diseases

OMIM ID
153640
OMIM term:
FECHTNER SYNDROME; FTNS
Alternative terms:
MACROTHROMBOCYTOPENIA, NEPHRITIS, DEAFNESS, AND LEUKOCYTE INCLUSIONS
ALPORT SYNDROME WITH MACROTHROMBOCYTOPENIA, FORMERLY; APSM, FORMERLY
(∗) Location:
22q12.3  
(†) Associated OMIM genes:
MYH9  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/jeh393jl