Disease #05971 (NERIB (neurodegeneration, infantile-onset, biotin-responsive (NERIB)), OMIM:618973)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	NERIB
Name	neurodegeneration, infantile-onset, biotin-responsive (NERIB)
OMIM ID	618973
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SLC5A6
Associated tissues	-
Disease features	-
Remarks	-
Date created	2021-10-06 15:19:33 +02:00 (CEST)
Date last edited	N/A

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