Disease #07057 (NEDMLOB (neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities), OMIM:620428)

Global Variome shared LOVD

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

Official abbreviation	NEDMLOB
Name	neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities
OMIM ID	620428
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CPSF3L
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-12-24 13:37:16 +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.