Phenotype #0000274566

Individual ID 00380713
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 2021-08-19 21:07:34 +02:00 (CEST)
Date last edited 2021-08-23 11:11:29 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.