Phenotype #0000059614
Individual ID |
00079918 |
Associated disease |
SLS |
Phenotype details |
HP:0007503 (Generalized Ichthyosis, severe); HP:0000989 (Pruritus, severe); HP:0001257 (Spasticity, severe); HP:0001249 (intellectual disability, IQ 55); HP:0030507 (retinal crystals); HP:0000613 (photophobia); HP:0001622 (premature birth, 38 weeks); HP:0002188 (Delayed CNS myelination) |
Diagnosis/Initial |
- |
Inheritance |
Familial, autosomal recessive |
Diagnosis/Definite |
- |
Age/Examination |
09y (9 years) |
Age/Diagnosis |
- |
Age/Onset |
- |
Phenotype/Onset |
- |
Protein |
- |
Owner name |
Maximilian Weustenfeld |
Database submission license |
No license selected |
Created by |
Maximilian Weustenfeld |
Date created |
2016-08-27 17:50:15 +02:00 (CEST) |
Date last edited |
2016-08-27 18:23:58 +02:00 (CEST) |
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