Phenotype #0000338912

Individual ID 00449751
Associated disease ID
Diagnosis/Initial behavioral abnormality
Diagnosis/Definite NECRC
Inheritance Isolated (sporadic)
Phenotype details HP:0001256, HP:0100259, HP:0000739, HP:0010526, HP:0010522, HP:0002354
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Marketa Wayhelova
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Marketa Wayhelova
Date created 2024-05-10 13:51:57 +02:00 (CEST)
Date last edited 2024-08-20 16:08:24 +02:00 (CEST)

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