Phenotype #0000223172

Individual ID 00295607
Associated disease HHF3
Phenotype details ORPHA:79299
HP:0005978
HP:0008283
HP:0001988
HP:0001985
HP:0000825
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Fanny Kortüm
Database submission license No license selected
Created by Fanny Kortüm
Date created 2020-03-18 11:30:51 +01:00 (CET)
Date last edited 2020-03-19 15:13:39 +01:00 (CET)

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