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Metadata
ID DOID:0070644
Name hereditary spastic paraplegia 92
Definition A hereditary spastic paraplegia that has_material_basis_in homozygous or compound heterozygous mutation in the FICD gene on chromosome 12q23.
https://pubmed.ncbi.nlm.nih.gov/36136088/
Xrefs

MIM:620911

SKOS

exactMatch MIM:620911

Subsets

DO_rare_slim

Synonyms

autosomal recessive spastic paraplegia 92 [EXACT]

SPG92 [EXACT]

Parent Relationships

is_a hereditary spastic paraplegia

is_a autosomal recessive disease

Subclass Logical Relationships

has material basis in some autosomal recessive inheritance

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