Disease #01718 (Jalili (Jalili syndrome), OMIM:217080)

Official abbreviation Jalili
Name Jalili syndrome
OMIM ID 217080
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene CNNM4
Associated tissues -
Disease features autosomal recessive
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

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     
00155447 - Sharon, submitted - F yes Israel Arab-Muslim - - - - Jalili - CNNM4 CNNM4 1 1 Dror Sharon
00155448 MOL0367 PubMed: Beryozkin 2015, PubMed: Sharon 2019 family F yes Israel Druze - - - - Jalili - CNNM4 CNNM4 1 1 Dror Sharon
Legend   How to query  


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