Disease #00836 (MRXS14 (intellectual developmental disorder, X-linked syndromic, type 14), OMIM:300676)

Global Variome shared LOVD

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Official abbreviation	MRXS14
Name	intellectual developmental disorder, X-linked syndromic, type 14
OMIM ID	300676
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	UPF3B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2026-08-28 16:16:36 +02:00 (CEST)

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