Disease #06437 (MRT68 (intellectual developmental disorder, autosomal recessive, type 68), OMIM:618302)

Official abbreviation	MRT68
Name	intellectual developmental disorder, autosomal recessive, type 68
OMIM ID	618302
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TRMT1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-12-10 23:20:41 +01:00 (CET)
Date last edited	2023-11-14 21:28:47 +01:00 (CET)

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Global Variome shared LOVD