Disease #00595 (HCH (hypochondroplasia (HCH)), OMIM:146000)

Official abbreviation HCH
Name hypochondroplasia (HCH)
OMIM ID 146000
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene FGFR3
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-10-22 16:16:54 +02:00 (CEST)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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     
00306132 66 - - M - China - - - - - HCH - FGFR3 FGFR3 1 1 Sha Hong
00449785 - - - - - - - - - - - HCH - FGFR3 FGFR3 1 1 Dan Feng Fang
00449786 - - - - - - - - - - - HCH - FGFR3 FGFR3 1 1 Dan Feng Fang
Legend   How to query  


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