Disease #07253 (SPAX11 (ataxia, spastic, type 11, autosomal dominant), OMIM:621226)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	SPAX11
Name	ataxia, spastic, type 11, autosomal dominant
OMIM ID	621226
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TUBA4A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2026-04-01 11:06:26 +02:00 (CEST)
Date last edited	N/A

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