Phenotype #0000060799

Individual ID 00081221
Associated disease SPG64
Phenotype details spasticity (HP:0001257), hyperreflexia (HP:0001347), Babinski sign (HP:0003487), intellectual disability, borderline (HP:0006889), delayed puberty (HP:0000823), microcephaly (HP:0000252)
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite -
Age/Examination 10y (10 years)
Age/Diagnosis 04y
Age/Onset 04y
Phenotype/Onset Gait disturbance (HP:0001288)
Protein -
Owner name Wietske Wesseling
Database submission license No license selected
Created by Wietske Wesseling
Date created 2016-09-25 12:49:29 +02:00 (CEST)
Date last edited 2017-01-06 13:11:44 +01:00 (CET)

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