Phenotype #0000060845
Individual ID |
00081268 |
Associated disease |
SLS |
Phenotype details |
HP:0007503 (Generalized Ichthyosis); HP:0000989 (Pruritus); HP:0000982 (Palmoplantar keratoderma); HP:0001264 (Spastic diplegia, moderate); Motor disability in arms (mild); HP:0005656 (Positional foot deformity, mild); HP:0001249 (intellectual disability, mild, no speech disorder!); HP:0001250 (seizures); HP:0030507 (retinal crystals); HP:0000613 (photophobia) |
Diagnosis/Initial |
- |
Inheritance |
Familial, autosomal recessive |
Diagnosis/Definite |
- |
Age/Examination |
23y (23 years) |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Maximilian Weustenfeld |
Database submission license |
No license selected |
Created by |
Maximilian Weustenfeld |
Date created |
2016-09-27 19:11:58 +02:00 (CEST) |
Date last edited |
N/A |
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