loading...| Preferred Name |
Cronkhite-Canada syndrome |
|
| Synonyms |
Gastrointestinal polyposis-ectodermal changes syndrome |
|
| Definitions |
Cronkhite-Canada syndrome (CCS) is a rare gastrointestinal (GI) polyposis syndrome characterized by the association of non-hereditary GI polyposis with the cutaneous triad of alopecia, nail changes and hyperpigmentation. |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_2930 |
|
| alternative_term |
Gastrointestinal polyposis-ectodermal changes syndrome Gastrointestinal polyposis-skin pigmentation-alopecia-fingernail changes syndrome |
|
| definition |
Cronkhite-Canada syndrome (CCS) is a rare gastrointestinal (GI) polyposis syndrome characterized by the association of non-hereditary GI polyposis with the cutaneous triad of alopecia, nail changes and hyperpigmentation. |
|
| definition_citation |
Orphanet |
|
| expertlink |
https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=2930 |
|
| has_age_of_onset |
Adult Elderly |
|
| has_inheritance |
Not applicable |
|
| hasDbXref |
ICD-10:D12.6 ICD-11:LD27.01 UMLS:C0282207 OMIM:175500 MedDRA:10062907 |
|
| label |
Cronkhite-Canada syndrome |
|
| notation |
ORPHA:2930 |
|
| part_of | ||
| prefixIRI |
ORDO:Orphanet_2930 |
|
| prefLabel |
Cronkhite-Canada syndrome |
|
| present_in |
Worldwide AND has_cases/families_value : 500.0 (Case) Worldwide AND has_point_prevalence_range : Unknown |
|
| treeView | ||
| subClassOf |