Individual #00091680

ID_report -
Reference PubMed: Tarailo-Graovac 2016, Journal: Tarailo-Graovac 2016
Remarks -
Gender -
Consanguinity -
Country United States
Population -
Age at death -
VIP -
Data_av -
Treatment -
Panel size 1
Diseases CA5AD
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 2016-12-12 22:51:01 +01:00 (CET)
Date last edited N/A


Phenotypes

deficiency, carbonic anhydrase VA, hyperammonemia (CA5AD) (CA5AD)   Add phenotype for this disease

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     
0000070124 neonatal hyperammonemia, hyperlactatemia, hypoglycemia; mild IDD; hyperammonemia, hyperlactatemia, hypoglycemia, PCC and 3MCC deficiency metabolites - - Familial, autosomal recessive - - - - - Johan den Dunnen



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000091823 DNA SEQ - - CA5A Not yet submitted Johan den Dunnen



Variants

Stop! No entries found!


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