Phenotype #0000272133

Individual ID 00376932
Associated disease WS1
Phenotype details -
Diagnosis/Initial -
Inheritance Familial, autosomal dominant
Diagnosis/Definite -
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Karina Lezirovitz Mandelbaum
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Karina Lezirovitz Mandelbaum
Date created 2021-06-26 16:10:39 +02:00 (CEST)
Date last edited 2021-06-28 09:06:26 +02:00 (CEST)

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