Disease #04386 (PRLTS5 (Perrault syndrome, type 5 (PRLTS5)), OMIM:616138)

Official abbreviation PRLTS5
Name Perrault syndrome, type 5 (PRLTS5)
OMIM ID 616138
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 C10orf2
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00056387 - PubMed: Demain 2016, Journal: Demain 2016 2-generation family, 1 affected, unaffected heterozygous carrier parents F - United Kingdom (Great Britain) Norwegian - - - - PRLTS5 see paper; ... C10orf2 C10orf2 2 1 Leigh Demain
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