Disease #03982 (MRT38 (mental retardation, autosomal recessive, type 38 (MRT38)), OMIM:615516)

Official abbreviation MRT38
Name mental retardation, autosomal recessive, type 38 (MRT38)
OMIM ID 615516
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 HERC2
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-05-17 13:27:38 +02:00 (CEST)


Individuals

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00081051 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MRT38 Mental retardation, autosomal recessive 38 (OMIM:615516) HERC2 HERC2 1 1 Daniel Trujillano
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