Disease #02732 (MCDR2 (dystrophy, macular, retinal, type 2 (MCDR2, Bull's eye macular dystrophy)), OMIM:608051)

Official abbreviation MCDR2
Name dystrophy, macular, retinal, type 2 (MCDR2, Bull's eye macular dystrophy)
OMIM ID 608051
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene PROM1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-07-28 14:30:25 +02:00 (CEST)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00032827 - PubMed: Michaelides 2003 - - - United Kingdom (Great Britain) British - - - - MCDR2 - PROM1 PROM1 1 10 Pascal Escher
00032829 - Michaelides et al., Submitted - - - United Kingdom (Great Britain) British - - - - MCDR2 - PROM1 PROM1 1 3 Pascal Escher
00382142 325 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - MCDR2 retinal dystrophy; MIM, 608051 PROM1 PROM1 1 1 LOVD
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.