Disease #00833

Official abbreviation MRX-15
Name mental retardation, X-linked, syndromic, type 15 (MRX-15, Cabezas type)
OMIM ID 300354
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 11
Phenotype entries for this disease 11
Associated with 1 gene CUL4B
Associated tissues -
Disease features -
Remarks -


Individuals

11 entries on 1 page. Showing entries 1 - 11.
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00022446 - - - M no Netherlands Caucasian - 0 yes - MRX-15 - CUL4B CUL4B 1 3 Anneke Vulto-van Silfhout
00022447 - - - M ? Germany - - 0 yes - MRX-15 - - CUL4B 1 3 Anneke Vulto-van Silfhout
00022448 - - - M - (France) - - 0 - - MRX-15 - - CUL4B 1 3 Anneke Vulto-van Silfhout
00022449 - - - M - - - - 0 - - MRX-15 - - CUL4B 1 1 Anneke Vulto-van Silfhout
00022450 - - - M - - - - 0 - - MRX-15 - CUL4B CUL4B 1 1 Anneke Vulto-van Silfhout
00022451 - - - - - - - - 0 - - MRX-15 - - CUL4B 1 1 Anneke Vulto-van Silfhout
00022452 - - - M - - - - 0 - - MRX-15 - CUL4B CUL4B 1 1 Anneke Vulto-van Silfhout
00022453 - - - - - - - - 0 - - MRX-15 - - CUL4B 1 2 Anneke Vulto-van Silfhout
00022454 - - - - - - - - 0 - - MRX-15 - CUL4B CUL4B 1 1 Anneke Vulto-van Silfhout
00022455 - - - - - - - - 0 - - MRX-15 - - CUL4B 1 2 Anneke Vulto-van Silfhout
00022456 - - - - - - - - 0 - - MRX-15 - - CUL4B 1 1 Anneke Vulto-van Silfhout
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