Disease #01066 (MRXSSD (mental retardation syndrome, X-linked, Siderius type (MRXSSD)), OMIM:300263)

Official abbreviation MRXSSD
Name mental retardation syndrome, X-linked, Siderius type (MRXSSD)
OMIM ID 300263
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 PHF8
Associated tissues -
Disease features X-linked
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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00433442 252731 - - M no Germany - - - - - MRXSSD Neurodevelopmental delay, Focal-onset seizure, Obesity, Polyphagia PHF8 PHF8 1 1 Andreas Laner
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