BabelNet

bn:05023755n

Noun Concept

No term available

Hereditary spastic paraplegia that is characterized by slowly progressive onset, usually between 18-60 years of age, and generally more severe spasticity and has material basis in mutation in the SPG7 gene on chromosome 16q24 Wikidata

Relations

Sources

IS A

doença rara

atrofia cerebral

paraparesia espástica familiar

doença autossómica recessiva

GENETIC ASSOCIATION

SPG7

HEALTH SPECIALTY

neurologia