Disease #00788 (MRXSL (mental retardation, X-linked syndromic, Lubs type (MRXSL)), OMIM:300260)

Official abbreviation MRXSL
Name mental retardation, X-linked syndromic, Lubs type (MRXSL)
OMIM ID 300260
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene MECP2
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

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00401514 135P - - M no Spain - - - - - ID, MRXS13, MRXSL - - MECP2 1 1 Alejandro Brea-Fernández
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