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Metadata
ID DOID:0070460
Name hereditary spastic paraplegia 90B
Definition A hereditary spastic paraplegia characterized by motor impairment and progressive lower limb spasticity that has_material_basis_in homozygous mutation in the SPTSSA gene on chromosome 14q13.1.
https://pubmed.ncbi.nlm.nih.gov/36718090/
Xrefs

MIM:620417

SKOS

exactMatch MIM:620417

Synonyms

autosomal recessive spastic paraplegia 90B [EXACT]

SPG90B [EXACT]

Parent Relationships

is_a autosomal dominant disease

is_a hereditary spastic paraplegia

Subclass Logical Relationships

has material basis in some autosomal dominant inheritance

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