Disease #01113 (MCCRP1 (microcephaly and chorioretinopathy, autosomal recessive, type 1 (MCCRP-1)), OMIM:251270)

Official abbreviation MCCRP1
Name microcephaly and chorioretinopathy, autosomal recessive, type 1 (MCCRP-1)
OMIM ID 251270
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 2
Associated with 1 gene TUBGCP6
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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00408981 10 PubMed: Puffenberger 2012 no patient number in publication, consecutive numbers given F - - Old Order Amish and Mennonite - - - - MCCRP1 congenital pachygyric microcephaly; global developmental delay; chorioretinopathy and retinal detachment TUBGCP6 TUBGCP6 1 1 LOVD
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