Disease #00827 (MRX90 (mental retardation, X-linked, type 90 (MRX90)), OMIM:300850)

Official abbreviation MRX90
Name mental retardation, X-linked, type 90 (MRX90)
OMIM ID 300850
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene DLG3
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-05-11 17:07:41 +02:00 (CEST)


Individuals

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00246685 00002 - - M - China - - - - - MRX90 severe developmental delay, cognitive impairment, could neither talk nor crawl. DLG3 - - 1 Xia Zhang
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