Disease #05867 (FADS2 (akinesia, fetal, deformation sequence, type 2 (FADS2)), OMIM:618388)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	FADS2
Name	akinesia, fetal, deformation sequence, type 2 (FADS2)
OMIM ID	618388
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	RAPSN
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-10-27 12:55:08 +01:00 (CET)
Date last edited	N/A

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