Disease #00840 (XLID109 (intellectual developmental disorder, X-linked, type 109 (FRAXE type)), OMIM:309548)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	XLID109
Name	intellectual developmental disorder, X-linked, type 109 (FRAXE type)
OMIM ID	309548
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	AFF2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2024-10-24 11:23:59 +02:00 (CEST)

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