Disease #00804 (MRT15 (mental retardation, autosomal recessive, type 15 (MRT-15)), OMIM:614202)

Official abbreviation MRT15
Name mental retardation, autosomal recessive, type 15 (MRT-15)
OMIM ID 614202
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 MAN1B1
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

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00327001 174406 - - F - - Arabia - - - - MRT15 (+) Neurodevelopmental delay, brother aslo affected MAN1B1 MAN1B1 1 1 Andreas Laner
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