Disease #01253 (CCD (dysplasia, cleidocranial (CCD)), OMIM:119600)

Official abbreviation CCD
Name dysplasia, cleidocranial (CCD)
OMIM ID 119600
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 7
Phenotype entries for this disease 5
Associated with 1 gene RUNX2
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

7 entries on 1 page. Showing entries 1 - 7.
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00079877 - - - - - Germany - - - - - CCD - RUNX2 RUNX2 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00117409 ? - - - - Argentina Latin American - - - - CCD cleidocranial dysplasia RUNX2 RUNX2 1 1 Ariel I Suarez
00132208 - - - - - Germany - - - - - CCD - RUNX2 RUNX2 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00163991 - - - - - - - - - - - CCD - RUNX2 RUNX2 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00359447 - - - - - (Brazil) - - - - - CCD - - RUNX2 1 1 Cynthia Silveira
00359448 - - - - - (Brazil) - - - - - CCD - - RUNX2 1 1 Cynthia Silveira
00359453 - - - - - (Brazil) - - - - - CCD - - RUNX2 1 1 Cynthia Silveira
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