Disease #07044 (XLID111 (intellectual developmental disorder, X-linked, type 111), OMIM:301107)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

Official abbreviation	XLID111
Name	intellectual developmental disorder, X-linked, type 111
OMIM ID	301107
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	X-linked
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SLITRK2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-11-14 17:20:47 +01:00 (CET)
Date last edited	N/A

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.