Disease #02690 (CMT1D (Charcot-Marie-Tooth disease, type ID (CMT-1D)), OMIM:607678)

Official abbreviation CMT1D
Name Charcot-Marie-Tooth disease, type ID (CMT-1D)
OMIM ID 607678
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene EGR2
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     
00315495 170351 - - M ? Germany - - - - - CMT1D Duane anomaly, Muscular hypotonia, Motor delay EGR2 EGR2 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.