hereditary spastic paraplegia 92

Term ID

DOID:0070644

Synonyms

autosomal recessive spastic paraplegia 92
SPG92

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/

References

MIM:620911

Ontology

Human Disease ( DOID:0070644 )

Relationships

is a type of: autosomal recessive disease hereditary spastic paraplegia

autosomal recessive disease hereditary spastic paraplegia Show first 5 Terms

Other Pages

Alliance (1)

Genes Involved

Zebrafish Models