Disease #01253

Official abbreviation CCD
Name dysplasia, cleidocranial (CCD)
OMIM ID 119600
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 4
Phenotype entries for this disease 2
Associated with 1 gene RUNX2
Associated tissues -
Disease features -
Remarks -


Individuals

4 entries on 1 page. Showing entries 1 - 4.
Legend  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age/Death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00079877 - - - - - Germany - - 0 - - CCD - RUNX2 RUNX2 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00117409 ? - - - - Argentina Latin American - 0 - - CCD cleidocranial dysplasia RUNX2 RUNX2 1 1 Ariel I Suarez
00132208 - - - - - Germany - - 0 - - CCD - RUNX2 RUNX2 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00163991 - - - - - - - - 0 - - CCD - RUNX2 RUNX2 1 1 Gemeinschaftspraxis für Humangenetik Dresden
Legend