All diseases

OMIM ID
108985
OMIM term:
SVEINSSON CHORIORETINAL ATROPHY; SCRA
Alternative terms:
ATROPHIA AREATA; AA
PERIPAPILLARY CHORIORETINAL DEGENERATION, ICELANDIC TYPE
HELICOIDAL PERIPAPILLARY CHORIORETINAL DEGENERATION; HPCD
(∗) Location:
11p15.3-p15.2  
(†) Associated OMIM genes:
TEAD1  
(‡) Associated MGI genes:

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