Disease #06848 (MRXS33 (Mental retardation, X-linked, syndromic 33), OMIM:300966)

Official abbreviation MRXS33
Name Mental retardation, X-linked, syndromic 33
OMIM ID 300966
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene TAF1
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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00431534 213999 - - M ? Turkey - - - - - MRXS33 Coloboma, Microcephaly, Pendular nystagmus, Delayed speech and language development, Autistic behavior TAF1 TAF1 1 1 Andreas Laner
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