Phenotype #0000141835

Individual ID 00177023
Associated disease EE
Phenotype details HP:0008936
HP:0002313
HP:0005348
HP:0007028
HP:0007337
HP:0006811
HP:0002469
HP:0000340
HP:0002705
HP:0005257
HP:0000767
HP:0001212
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite Epileptic encephalopathy, early infantile, 4
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset HP:0003623
Protein -
Owner name Anaïs Begemann
Database submission license No license selected
Created by Anaïs Begemann
Date created 2018-08-16 16:26:55 +02:00 (CEST)
Date last edited 2018-08-17 11:40:06 +02:00 (CEST)

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