Disease #01722 (MCD (dystrophy, macular, corneal (MCD)), OMIM:217800)

Official abbreviation MCD
Name dystrophy, macular, corneal (MCD)
OMIM ID 217800
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 CHST6
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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00106630 26604660-Pat5-1/5-2 PubMed: Park 2015 - F - Korea, South (Republic) - - - - - MCD Macular corneal dystrophy CHST6 CHST6 2 2 Hyojin Chae
00106631 26604660-Pat6 PubMed: Park 2015 - F - Korea, South (Republic) - - - - - MCD Macular corneal dystrophy CHST6 CHST6 2 1 Hyojin Chae
00106632 26604660-Pat2 PubMed: Park 2015 - F - Korea, South (Republic) - - - - - MCD Macular corneal dystrophy CHST6 CHST6 2 1 Hyojin Chae
00106671 26604660-Pat1 PubMed: Park 2015 - M - Korea, South (Republic) - - - - - MCD - CHST6 CHST6 2 1 Hyojin Chae
00106672 26604660-Pat3 PubMed: Park 2015 - M - Korea, South (Republic) - - - - - MCD - CHST6 CHST6 2 1 Hyojin Chae
00106673 26604660-Pat4 PubMed: Park 2015 - M - Korea, South (Republic) - - - - - MCD - CHST6 CHST6 2 1 Hyojin Chae
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