http://caligraph.org/ontology/Neurogenetic_disorder

CaLiGraph

Property	Value
rdf:type	owl:Class
rdfs:label	Neurogenetic disorder
rdfs:subClassOf	Congenital disorder of nervous system Genetic disease or disorder
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Category:Neurogenetic_disorders
is rdf:type of	Fragile X syndrome Roussy–Lévy syndrome Tourette syndrome Spinal muscular atrophy with lower extremity predominance 1 Hereditary sensory and autonomic neuropathy Spinal muscular atrophy McLeod syndrome FBXW7 neurodevelopmental syndrome Kohlschütter-Tönz syndrome Pontocerebellar hypoplasia Spinal muscular atrophy with progressive myoclonic epilepsy Hereditary sensory and autonomic neuropathy type I Dentatorubral–pallidoluysian atrophy Neotenic complex syndrome Hereditary motor and sensory neuropathy Mandibulofacial dysostosis-microcephaly syndrome Distal spinal muscular atrophy type 1 Neurogenetic disorders Dejerine–Sottas disease Spinal muscular atrophy with lower extremity predominance 2A Allan–Herndon–Dudley syndrome GLUT1 deficiency Congenital distal spinal muscular atrophy Spinal muscular atrophy with lower extremity predominance 2B

About: clgo:Neurogenetic_disorder