Disease #00105 (FSNF (NEUROFIBROMATOSIS, FAMILIAL SPINAL), OMIM:162210)

MVZ für Humangenetik Regensburg

LOVD v.3.0 Build 30 [ Current LOVD status ]
Log in

	Curator: Florian Bayersdorfer

Official abbreviation	FSNF
Name	NEUROFIBROMATOSIS, FAMILIAL SPINAL
OMIM ID	162210
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NF1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2023-06-16 09:46:43 +00:00 (UTC)
Date last edited	N/A