Disease #06981 (NOC (neuroocular syndrome), OMIM:619539)

Official abbreviation NOC
Name neuroocular syndrome
OMIM ID 619539
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene PRR12
Associated tissues -
Disease features -
Remarks -
Date created 2022-11-30 16:21:49 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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     
00426469 209706 - - F no Germany - - - - - NOC neurodevelopmental delay, delayed speech and language development PRR12 PRR12 1 1 Andreas Laner
00427165 210060 - - M no Germany - - - - - NOC Neurodevelopmental delay, Hypotonia, Hearing impairment PRR12 PRR12 1 1 Andreas Laner
Legend   How to query  


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