camptodactyly-arthropathy-coxa vara-pericarditis syndrome
about
P2293
CACP, encoding a secreted proteoglycan, is mutated in camptodactyly-arthropathy-coxa vara-pericarditis syndromeThe camptodactyly-arthropathy-coxa vara-pericarditis syndrome: clinical features and genetic mapping to human chromosome 1.Camptodactyly-arthropathy-coxa vara-pericarditis syndrome: important differential for juvenile idiopathic arthritis.The Efficacy of Yttrium-90 Radiosynovectomy in Patients with Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome.Total hip arthroplasty in adolescents with severe hip arthropathy and dysplasia associated with camptodactyly-arthropathy-coxa vara-pericarditis syndrome.Camptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome with Shoulder Joint Involvement: A Case Report with Literature Review.A novel mutation in PRG4 gene underlying camptodactyly-arthropathy-coxa vara-pericarditis syndrome with the possible expansion of the phenotype to include congenital cataractCamptodactyly-Arthropathy-Coxa Vara-Pericarditis Syndrome Versus Juvenile Idiopathic ArthropathyClinical variability and genetic homogeneity of the camptodactyly-arthropathy-coxa vara-pericarditis syndromeSynovial pathology in camptodactyly-arthropathy-coxa vara-pericarditis syndromeA novel deletion mutation in proteoglycan-4 underlies camptodactyly-arthropathy-coxa-vara-pericarditis syndrome in a consanguineous pakistani family[Camptodactyly-Arthropathy-Coxa-Vara-Pericarditis syndrome: a case report]
P921
Q22010750-835DBE21-895C-48A8-BCBE-078DE4B0FCF4Q34464837-BE372BBF-8817-4009-93A8-B942612F705EQ37188423-8511EBF2-8032-447C-A5B9-CC2E53AFC739Q42316448-674BC5B8-D571-4CD3-B246-85CF5BF06355Q43967599-E761CB7F-C655-40A5-A5D1-DD1731D2686AQ53712555-0BBA1621-7F1A-4837-BDF2-1C81229F8B2BQ56787155-0B3E73D5-2982-4208-ACA7-E8B0FBCC1D72Q61855412-01D7D37B-6D74-45FF-A791-73DCA94B6620Q63681427-6BAC3536-9C96-4728-913D-B8B85AD43E0EQ81384223-7A251674-B9D7-4F5F-8353-0137619B3F0AQ84085384-37CC683A-849D-4B74-86BE-C0EC66C23070Q84955848-65FEAA89-0F81-4C13-A3E2-9ACC5B76BF27
P921
camptodactyly-arthropathy-coxa vara-pericarditis syndrome
description
human disease
@en
name
camptodactyly-arthropathy-coxa vara-pericarditis syndrome
@en
syndrome de camptodactylie-arthropathie-coxa vara-péricardite
@fr
type
label
camptodactyly-arthropathy-coxa vara-pericarditis syndrome
@en
syndrome de camptodactylie-arthropathie-coxa vara-péricardite
@fr
altLabel
Arthropathy camptodactyly syndrome
@en
CACP syndrome
@en
CACP
@en
CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME
@en
CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME; CACP
@en
CAP syndrome
@en
Camptodactyly arthropathy coxa vara pericarditis syndrome
@en
Camptodactyly arthropathy pericarditis syndrome
@en
Camptodactyly-arthropathy-coxa-vara-pericarditis syndrome
@en
Fibrosing serositis, familial
@en
prefLabel
camptodactyly-arthropathy-coxa vara-pericarditis syndrome
@en
syndrome de camptodactylie-arthropathie-coxa vara-péricardite
@fr
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P5270
MONDO:0008828
P699
DOID:0090127