Phenotype #0000106395

Individual ID 00133645
Associated disease PCH9
Phenotype details Sleep disturbance (HP:0002360), postprandial hyperglycemia (HP:0011998), gastroesophageal reflux (HP:0002020)
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
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 2017-11-15 21:47:32 +01:00 (CET)
Date last edited 2017-11-17 14:31:28 +01:00 (CET)

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