Phenotype #0000302843

Individual ID 00410752
Associated disease AAAS
Phenotype details see paper; ..., lacrima, achalasia, anejaculation, optic atrophy, muscle weakness, dysarthria, autonomic dysfunction
Diagnosis/Initial Allgrove syndrome
Inheritance Familial, autosomal recessive
Diagnosis/Definite AAAS
Age/Examination 29y (29 years)
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2022-05-30 13:14:37 +02:00 (CEST)
Date last edited N/A

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