Disease #06849 (MRXS99F (Mental retardation, X-linked 99, syndromic, female-restricted), OMIM:300968)

Official abbreviation MRXS99F
Name Mental retardation, X-linked 99, syndromic, female-restricted
OMIM ID 300968
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene USP9X
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

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00435031 254088 - - F no Germany - - - - - MRXS99F Gait disturbance, Pes cavus, Scoliosis, Abnormality of eye movement, Brain imaging abnormality, Scheuermann-like vertebral changes USP9X USP9X 1 1 Andreas Laner
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