Arthropathy

Symptom Information:

Symptom ID: HPO:0003040
Synonyms:
Arthropathy [OMIM:Arthropathy]
Arthropathy (onset third-fourth decade) [OMIM:Arthropathy (onset third-fourth decade)]
Arthropathy [MedDRA:10003285]
Quality:
Cross references:
OMIM: "Arthropathy" [OMIM:Arthropathy]
OMIM: "Arthropathy (onset third-fourth decade)" [OMIM:Arthropathy (onset third-fourth decade)]
UMLS:C0022408 "Arthropathy" [HPO:0003040]
Is a (Direct Parents):
MedDRA Arthropathies NEC
HPO         Abnormal joint morphology
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal joint morphology(HPO:0001367)
                Arthropathy(HPO:0003040)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Joint disorders(MedDRA:10023213)
       Arthropathies NEC(MedDRA:10003284)
          Arthropathy(HPO:0003040)
Database Frequency: 19 / 7739
Resource:

All diseases associated with this symptom:

Alkaptonuria (Orphanet:56)
CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME (OMIM:208250)
CHONDROCALCINOSIS 2 (OMIM:118600)
CHONDROCALCINOSIS DUE TO APATITE CRYSTAL DEPOSITION (OMIM:118610)
CHST3-related skeletal dysplasia (Orphanet:263463)
Cranio-osteoarthropathy (Orphanet:1525)
Familial articular chondrocalcinosis (Orphanet:1416)
Familial digital arthropathy-brachydactyly (Orphanet:85169)
Hemochromatosis type 4 (Orphanet:139491)
Hemochromatosis, type 1 (OMIM:235200)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Mucopolysaccharidosis type 2 (Orphanet:580)
Progressive pseudorheumatoid arthropathy of childhood (Orphanet:1159)
STICKLER SYNDROME, TYPE I (OMIM:108300)
Scheie syndrome (Orphanet:93474)
Stickler syndrome (Orphanet:828)
Stickler syndrome type 2 (Orphanet:90654)
WINCHESTER SYNDROME (OMIM:277950)