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Metadata
ID	DOID:0110817
Name	hereditary spastic paraplegia 72A
Definition	A hereditary spastic paraplegia that has_material_basis_in a heterozygous mutation in the REEP2 gene on chromosome 5q31.2. https://www.ncbi.nlm.nih.gov/pubmed/24388663
Xrefs	ICD10CM:G11.4 MIM:615625 ORDO:401849
SKOS	broadMatch ORDO:401849 broadMatch ICD10CM:G11.4
Subsets	DO_rare_slim
Synonyms	SPG72 [EXACT]
Parent Relationships	is_a autosomal dominant disease is_a hereditary spastic paraplegia
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance