Disease #01125 (MRX63 (mental retardation, X-linked, type 63 (MRX63)), OMIM:300387)

Official abbreviation MRX63
Name mental retardation, X-linked, type 63 (MRX63)
OMIM ID 300387
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant
Individuals reported having this disease 2
Phenotype entries for this disease -
Associated with 1 gene ACSL4
Associated tissues -
Disease features -
Remarks -


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00392045 242P1 family, 2 affected - M no Spain - - - - - MRX63 - - ACSL4 1 2 Alejandro Brea-Fernández
00392046 242P2 - - M no Spain - - - - - MRX63 - - ACSL4 1 1 Alejandro Brea-Fernández
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