Phenotypes for disease #04047 (SPG64 (paraplegia, spastic, type 64, autosomal recessive (SPG-64)), OMIM:615683)

2 entries on 1 page. Showing entries 1 - 2.
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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     
0000060710 Spasticity (HP:0001257) Talipes equinovarus (HP:0001762) Hyperreflexia (HP:0001347) Babinski sign (HP:0003487) Skeletal muscle atrophy (HP:0003202) Aggressive behavior (HP:0000718) Delayed puberty (HP:0000823) Microcephaly (HP:0000252) Intellectual disability, borderline (HP:0006889) - - Unknown 15y - 03y06m Gait disturbance (HP:0001288) - Wietske Wesseling 00081212
0000060799 spasticity (HP:0001257), hyperreflexia (HP:0001347), Babinski sign (HP:0003487), intellectual disability, borderline (HP:0006889), delayed puberty (HP:0000823), microcephaly (HP:0000252) - - Familial, autosomal recessive 10y 04y 04y Gait disturbance (HP:0001288) - Wietske Wesseling 00081221
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