Disease #05260 (CAVIPMR (atrophy, cerebellar, visual impairment, psychomotor retardation (CAVIPMR)), OMIM:616875)

Official abbreviation CAVIPMR
Name atrophy, cerebellar, visual impairment, psychomotor retardation (CAVIPMR)
OMIM ID 616875
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene EMC1
Associated tissues -
Disease features -
Remarks -
Date created 2017-04-11 14:50:42 +02:00 (CEST)
Date last edited 2020-11-13 14:32:57 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00103210 proband - - M yes India Indian - - yes - CAVIPMR - EMC1 EMC1 1 1 MedGenome_db
00413461 FamHXPatI - - F no New Zealand NZ Maori/Samoan 07y - - - CAVIPMR - EMC1 EMC1 2 1 Sandra Cooper
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