Disease #07039 (NEDMILG (neurodevelopmental disorder with microcephaly, impaired language, gait abnormalities, autosomal recessive), OMIM:619091)

Official abbreviation	NEDMILG
Name	neurodevelopmental disorder with microcephaly, impaired language, gait abnormalities, autosomal recessive
OMIM ID	619091
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NARS
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-11-09 09:25:17 +01:00 (CET)
Date last edited	N/A

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Global Variome shared LOVD