Disease #07089 (XLID110 (intellectual developmental disorder, X-linked type 110), OMIM:301095)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	XLID110
Name	intellectual developmental disorder, X-linked type 110
OMIM ID	301095
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	FGF13
Associated tissues	-
Disease features	-
Remarks	-
Date created	2024-05-29 10:56:25 +02:00 (CEST)
Date last edited	N/A

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