Disease #02193 (OGDNS;NATD (Ogden syndrome (OGDNS, N-terminal acetyltransferase deficiency (NATD))), OMIM:300855)

Official abbreviation OGDNS;NATD
Name Ogden syndrome (OGDNS, N-terminal acetyltransferase deficiency (NATD))
OMIM ID 300855
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked dominant, X-linked recessive
Individuals reported having this disease 1
Phenotype entries for this disease -
Associated with 1 gene NAA10
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

1 entry on 1 page. Showing entry 1.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00060305 - - - F - - - - - - - ID, OGDNS;NATD - NAA10 NAA10 1 1 Bernt Popp
Legend   How to query  


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