Disease #04666 (MRT48 (mental retardation, autosomal recessive, type 48 (MRT-48)), OMIM:616269)

Official abbreviation MRT48
Name mental retardation, autosomal recessive, type 48 (MRT-48)
OMIM ID 616269
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 SLC6A17
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

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00465863 304 - - M yes Pakistan Asian - - - - MRT48 intellectual disbaility, short stature, developmental delay SLC6A17 SLC6A17 1 1 Malik Ali Asghar
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