Disease #03358 (MCOP6 (microphthalmia, isolated, type 6), OMIM:613517)

Official abbreviation MCOP6
Name microphthalmia, isolated, type 6
OMIM ID 613517
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PRSS56
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2025-12-27 15:33:39 +01:00 (CET)


Individuals

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00382092 260 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - MCOP6 microphthalmia, anophthalmia, and coloboma; MIM, 613517 PRSS56 PRSS56 1 1 LOVD
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