Global Variome shared LOVD

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Phenotype #0000060865 Individual ID 00081293 Associated disease SLS Phenotype details HP:0007503 (Generalized Ichthyosis, Extremities: severe, Trunk: severe); HP:0002313 (Spastic paraparesis, moderate, moderate gait abnormality); HP:0005750 (Contractures of the joints of the lower limbs, moderate) HP:0001249 (intellectual disability, mild); HP:0001260 (Dysarthria, mild); HP:0007663 (Reduced visual acuity, right: 6/36, left: 6/18); HP:0030507 (retinal crystals); HP:0000551 (Abnormality of color vision, moderate) Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination 19y (19 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Maximilian Weustenfeld Database submission license No license selected Created by Maximilian Weustenfeld Date created 2016-09-29 13:57:49 +02:00 (CEST) Date last edited N/A

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