Disease #00326 (MCOP8 (microphthalmia, isolated, type 8 (MCOP-8)), OMIM:615113)

Official abbreviation MCOP8
Name microphthalmia, isolated, type 8 (MCOP-8)
OMIM ID 615113
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 7
Phenotype entries for this disease 7
Associated with 1 gene ALDH1A3
Associated tissues -
Disease features -
Remarks -
Date created 2014-02-16 17:01:25 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00011463 - - - M yes Egypt - - - - - MCOP8 - ALDH1A3 ALDH1A3 1 4 Daniel Schorderet
00017708 - - - ? ? - - - - - - MCOP8 - ALDH1A3 ALDH1A3 1 1 Daniel Schorderet
00017709 - - - ? ? - - - - - - MCOP8 - ALDH1A3 ALDH1A3 1 1 Daniel Schorderet
00017710 - - - ? ? - - - - - - MCOP8 - ALDH1A3 ALDH1A3 1 1 Daniel Schorderet
00017711 - - - ? ? - - - - - - MCOP8 - ALDH1A3 ALDH1A3 1 1 Daniel Schorderet
00017712 - - - ? ? - - - - - - MCOP8 - ALDH1A3 ALDH1A3 1 1 Daniel Schorderet
00382088 25 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - MCOP8 microphthalmia, anophthalmia, and coloboma; MIM, 615113 ALDH1A3 ALDH1A3 2 1 LOVD
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