Disease #00723 (FSNF (neurofibromatosis, familial spinal), OMIM:162210)

Official abbreviation FSNF
Name neurofibromatosis, familial spinal
OMIM ID 162210
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene NF1
Associated tissues -
Disease features -
Remarks -