Disease #02208 (MRX100 (mental retardation, X-linked, type 100 (MRX100)), OMIM:300923)

Official abbreviation MRX100
Name mental retardation, X-linked, type 100 (MRX100)
OMIM ID 300923
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 KIF4A
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2020-05-11 15:17:27 +02:00 (CEST)


Individuals

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00472450 362577 - - M yes Syria - - - - - MRX100 Delayed speech and language development, Neurodevelopmental delay KIF4A KIF4A 1 1 Andreas Laner
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