Disease #00834 (MRX30;MRX47 (mental retardation, X-linked, type 30/47 (MRX30;MRX47)), OMIM:300558)

Official abbreviation MRX30;MRX47
Name mental retardation, X-linked, type 30/47 (MRX30;MRX47)
OMIM ID 300558
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene PAK3
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

2 entries on 1 page. Showing entries 1 - 2.
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00248348 - - 2-generation family, patient and unaffected heterozygous carrier mother M no Hungary - - - - - MRX30;MRX47 Intellectual disability (HP:0001249) Microcephaly (HP:0000252) PAK3 PAK3 1 1 Dora Nagy
00391861 026P - - F no Spain - - - - - ID, MRX30;MRX47 - - PAK3 1 1 Alejandro Brea-Fernández
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