Disease #00833 (MRXSC (Mental retardation, X-linked, syndromic 15 (Cabezas type)), OMIM:300354)

Official abbreviation MRXSC
Name Mental retardation, X-linked, syndromic 15 (Cabezas type)
OMIM ID 300354
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 13
Phenotype entries for this disease 12
Associated with 1 gene CUL4B
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

13 entries on 1 page. Showing entries 1 - 13.
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00022446 - - - M no Netherlands white - - yes - MRXSC - CUL4B CUL4B 1 3 Anneke Vulto-van Silfhout
00022447 - - - M ? Germany - - - yes - MRXSC - - CUL4B 1 3 Anneke Vulto-van Silfhout
00022448 - - - M - (France) - - - - - MRXSC - - CUL4B 1 3 Anneke Vulto-van Silfhout
00022449 - - - M - - - - - - - MRXSC - - CUL4B 1 1 Anneke Vulto-van Silfhout
00022450 - - - M - - - - - - - MRXSC - CUL4B CUL4B 1 1 Anneke Vulto-van Silfhout
00022451 - - - - - - - - - - - MRXSC - - CUL4B 1 1 Anneke Vulto-van Silfhout
00022452 - - - M - - - - - - - MRXSC - CUL4B CUL4B 1 1 Anneke Vulto-van Silfhout
00022453 - - - - - - - - - - - MRXSC - - CUL4B 1 2 Anneke Vulto-van Silfhout
00022454 - - - - - - - - - - - MRXSC - CUL4B CUL4B 1 1 Anneke Vulto-van Silfhout
00022455 - - - - - - - - - - - MRXSC - - CUL4B 1 2 Anneke Vulto-van Silfhout
00022456 - - - - - - - - - - - MRXSC - - CUL4B 1 1 Anneke Vulto-van Silfhout
00271297 ED2150 Ritelli et al., 2020 submitted - M no Italy - - - - - LFIT2, MRXSC, SOPH - CUL4B, NBAS CUL4B, NBAS 3 1 Marco Ritelli
00414789 203088 - - M no Germany - - - - - MRXSC Intellectual disability, mild, Sleep disturbance, Lipoma, EEG abnormality, Seizure CUL4B CUL4B 1 1 Andreas Laner
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