Disease #02932 (RCD3B (dystrophy, retinal cone, type 3B (RCD-3B)), OMIM:610356)

Official abbreviation RCD3B
Name dystrophy, retinal cone, type 3B (RCD-3B)
OMIM ID 610356
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 1 gene KCNV2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00155484 - Sharon, submitted - M yes Israel Yemenite;Jewish - - - - RCD3B - KCNV2 KCNV2 1 2 Dror Sharon
00155485 - Sharon, submitted - M no Israel Beduin - - - - RCD3B - KCNV2 KCNV2 1 2 Dror Sharon
00155486 - Sharon, submitted - M no Israel Jewish - - - - RCD3B - KCNV2 KCNV2 2 3 Dror Sharon
00155487 - Sharon, submitted - M yes Israel Yemenite;Jewish - - - - RCD3B - KCNV2 KCNV2 1 1 Dror Sharon
00155488 - Sharon, submitted - F no Israel Jewish - - - - RCD3B - KCNV2 KCNV2 2 2 Dror Sharon
00155489 - Sharon, submitted - F yes Israel Jewish-Oriental - - - - RCD3B - KCNV2 KCNV2 1 1 Dror Sharon
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