Phenotype #0000268944

Individual ID 00373719
Associated disease CSA
Phenotype details HP:0001276; HP:0001249; HP:0006817; HP:0000238; HP:0100702; HP:0001263; HP:0000750; HP:0001181; HP:0002194; HP:0010862; HP:0001883
Diagnosis/Initial -
Inheritance Familial, autosomal recessive
Diagnosis/Definite Cockayne syndrome, type A (OMIM 216400)
Age/Examination -
Age/Diagnosis -
Age/Onset -
Phenotype/Onset -
Protein -
Owner name Wenjuan Qiu
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Wenjuan Qiu
Date created 2021-05-19 07:09:55 +02:00 (CEST)
Date last edited 2021-05-28 13:21:28 +02:00 (CEST)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
  Powered by LOVD v.3.0 Build 30b
LOVD software ©2004-2024 Leiden University Medical Center
Database contents © by their respective submitters and curators
 There are currently no updates.