Disease #02723 (MCOPS6 (microphthalmia syndromic, type 6 (MCOPS-6)), OMIM:607932)

Official abbreviation MCOPS6
Name microphthalmia syndromic, type 6 (MCOPS-6)
OMIM ID 607932
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene BMP4
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

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00218415 - - - M no - European, Vietnamese - - - - MCOPS6 mild delayed milestones, delayed speech, mild hypotonia, dysmorphic features, macrocephaly, post axial polydactyly - BMP4 2 1 Patrick R. Blackburn
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