Disease #06590 (HIDEA (Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities), OMIM:618493)

Official abbreviation HIDEA
Name Hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities
OMIM ID 618493
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 6
Phenotype entries for this disease -
Associated with 1 gene P4HTM
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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     
00411161 - - - M yes Finland - - - - - HIDEA - - P4HTM 1 1 Elisa Rahikkala
00411162 - - - M yes Iran - - - - - HIDEA - - P4HTM 1 1 Elisa Rahikkala
00411163 - - - F no Finland - - - - - HIDEA - - P4HTM 1 1 Elisa Rahikkala
00411164 - - - F no Finland - - - - - HIDEA - - P4HTM 2 1 Elisa Rahikkala
00411165 - - - M yes France - - - - - HIDEA - - P4HTM 1 1 Elisa Rahikkala
00411166 - - - F yes Iran - - - - - HIDEA - - P4HTM 1 1 Elisa Rahikkala
Legend   How to query  


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