Disease #02332 (CORD5 (dystrophy, cone-rod, type 5 (CORD5)), OMIM:600977)

Official abbreviation CORD5
Name dystrophy, cone-rod, type 5 (CORD5)
OMIM ID 600977
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 35
Phenotype entries for this disease 35
Associated with 1 gene PITPNM3
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-11-03 17:11:25 +01:00 (CET)


Individuals

35 entries on 1 page. Showing entries 1 - 35.
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00324157 Fam151Pat18 PubMed: Balciuniene 1995, PubMed: Reinis 2012 5-generation family, 22 affected M - Sweden - >12y - - - CORD5 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), Color vision defect (HP:0000551) PITPNM3 PITPNM3 1 22 Mariah De Bruin
00324158 Fam151Pat17 PubMed: Reinis 2012 - M - Sweden - >25y - - - CORD5 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551) PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324159 Fam151Pat16 PubMed: Reinis 2012 - M - Sweden - >35y - - - CORD5 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551) PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324160 Fam151Pat15 PubMed: Reinis 2012 - F - Sweden - >26y - - - CORD5 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551) PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324161 Fam151Pat14 PubMed: Reinis 2012 - F - Sweden - >32y - - - CORD5 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551) PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324162 Fam151Pat13 PubMed: Reinis 2012 - F - Sweden - >32y - - - CORD5 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551) PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324163 Fam151Pat12 PubMed: Reinis 2012 - F - Sweden - >46y - - - CORD5 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551) PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324164 Fam151Pat11 PubMed: Reinis 2012 - M - Sweden - >32y - - - CORD5 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), color vision defect (HP:0000551) PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324165 Fam151Pat10 PubMed: Reinis 2012 - M - Sweden - >27y - - - CORD5 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), Color vision defect (HP:0000551) PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324166 Fam151Pat9 PubMed: Reinis 2012 - F - Sweden - >44y - - - CORD5 macular degeneration (HP:0000608), progressive visual loss (HP:0000529), Color vision defect (HP:0000551) PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324300 Fam151Pat8 PubMed: Reinis 2012 - M - Sweden - >53y - - - CORD5 color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324301 Fam151Pat7 PubMed: Reinis 2012 - F - Sweden - >72y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324302 Fam151Pat6 PubMed: Reinis 2012 - M - Sweden - >51y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324303 Fam151Pat5 PubMed: Reinis 2012 - F - Sweden - >60y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324304 Fam151Pat4 PubMed: Reinis 2012 - F - Sweden - >64y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324305 Fam151Pat3 PubMed: Reinis 2012 - M - Sweden - >69y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324306 Fam151Pat2 PubMed: Reinis 2012 - F - Sweden - >71y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324307 Fam151Pat1 PubMed: Reinis 2012 - F - Sweden - >75y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324326 Fam152Pat17 PubMed: Reinis 2012 7-generation family, 17 affected F - Sweden - >21y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 17 Mariah De Bruin
00324327 Fam152Pat16 PubMed: Reinis 2012 - M - Sweden - >17y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324328 Fam152Pat15 PubMed: Reinis 2012 - F - Sweden - >22y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324329 Fam152Pat14 PubMed: Reinis 2012 - M - Sweden - >08y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324330 Fam152Pat13 PubMed: Reinis 2012 - M - Sweden - >32y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324331 Fam152Pat12 PubMed: Reinis 2012 - M - Sweden - >35y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324332 Fam152Pat11 PubMed: Reinis 2012 - F - Sweden - >28y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324333 Fam152Pat10 PubMed: Reinis 2012 - F - Sweden - >36y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324334 Fam152Pat9 PubMed: Reinis 2012 - F - Sweden - >23y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324335 Fam152Pat8 PubMed: Reinis 2012 - F - Sweden - >44y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324336 Fam152Pat7 PubMed: Reinis 2012 - F - Sweden - >56y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324337 Fam152Pat6 PubMed: Reinis 2012 - F - Sweden - >56y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324387 Fam152Pat5 PubMed: Reinis 2012 - F - Sweden - >60y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324388 Fam152Pat4 PubMed: Reinis 2012 - F - Sweden - >59y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324389 Fam152Pat3 PubMed: Reinis 2012 - F - Sweden - >61y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324390 Fam152Pat2 PubMed: Reinis 2012 - F - Sweden - >63y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
00324391 Fam152Pat1 PubMed: Reinis 2012 - F - Sweden - >66y - - - CORD5 Color vision defect (HP:0000551), progressive visual loss (HP:0000529), macular degeneration HP:0000608 PITPNM3 PITPNM3 1 1 Mariah De Bruin
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