Disease #00056 (MJDS (MAJEED SYNDROME), OMIM:609628)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
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Official abbreviation	MJDS
Name	MAJEED SYNDROME
OMIM ID	609628
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	LPIN2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-02-05 11:31:28 +00:00 (UTC)
Date last edited	N/A