Disease #03886 (MRT36 (mental retardation, autosomal recessive, type 36 (MRT-36)), OMIM:615286)

Official abbreviation MRT36
Name mental retardation, autosomal recessive, type 36 (MRT-36)
OMIM ID 615286
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene ADAT3
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

3 entries on 1 page. Showing entries 1 - 3.
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00080884 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MRT36 Mental retardation, autosomal recessive 36 (OMIM:615286) ADAT3 ADAT3, SCAMP4 1 1 Daniel Trujillano
00080980 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MRT36 Mental retardation, autosomal recessive 36 (OMIM:615286) ADAT3 ADAT3, SCAMP4 1 1 Daniel Trujillano
00081076 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - MRT36 Mental retardation, autosomal recessive 36 (OMIM:615286) ADAT3 ADAT3, SCAMP4 1 1 Daniel Trujillano
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