Disease #03283 (SPG44 (paraplegia, spastic, type 44, autosomal recessive (SPG-44)), OMIM:613206)

Official abbreviation SPG44
Name paraplegia, spastic, type 44, autosomal recessive (SPG-44)
OMIM ID 613206
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene GJC2
Associated tissues -
Disease features -
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Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00055375 - - - - - Italy - - 0 - - SPG44 spastic paraplegia GJC2 GJC2 2 1 Michel van Geel
00231414 - - - - - - - - 0 - - SPG44 - GJC2 GJC2 2 1 Gemeinschaftspraxis für Humangenetik Dresden
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