Phenotypes for disease #02642 (SPG7 (paraplegia, spastic, autosomal recessive, type 7 (SPG-7)), OMIM:607259)

4 entries on 1 page. Showing entries 1 - 4.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000041527 pure ataxia only cerebellar ataxia SPG7 Familial, autosomal recessive - - 58y - - Erik-Jan Kamsteeg 00054863
0000041528 pure ataxia only cerebellar ataxia SPG7 Familial, autosomal recessive - - 38y - - Erik-Jan Kamsteeg 00054864
0000041529 HSP and ataxia, mild pyramidal signs lower limbs cerebellar ataxia SPG7 Familial, autosomal recessive - - 52y - - Erik-Jan Kamsteeg 00054865
0000296571 cerebellar ataxia Spastic lower limbs, hyperreflexia, intact abdominal reflexes peripheral neuropathy pes cavus HSP SPG-7 Familial, autosomal recessive 45y 38y - 33y - Sherifa Ahmed Hamed 00403898
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