Disease #03812 (HSAN9;SPG49 (neuropathy, hereditary sensory and autonomic, type IX, with developmental delay (SPG49)), OMIM:615031)

Global Variome shared LOVD

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Official abbreviation	HSAN9;SPG49
Name	neuropathy, hereditary sensory and autonomic, type IX, with developmental delay (SPG49)
OMIM ID	615031
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	TECPR2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2024-02-23 14:22:55 +01:00 (CET)

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