Arthropathy

An arthropathy is a disease of a joint. Signs and symptoms Joint pain is a common but non-specific sign of joint disease. [Source: Wikipedia ]

Subtypes
Arthritis
Cheiroarthropathy
May Be Caused by
Acromegaly
Al-Aqeel Sewairi syndrome
Alkaptonuria
Amyloidosis
Ankylosing spondylitis
Anti-Jo-1 antibody syndrome
Arthropathy-camptodactyly syndrome
Autosomal dominant premature degenerative osteoarthropathy of the hip
Beekeeper arthropathy
Behçet disease
Blau syndrome
Blind loop syndrome
Calcium pyrophosphate dihydrate crystal deposition disease
Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
Caplan syndrome
Chondrodysplasia punctata Conradi-Hünermann type
Chondrodysplasia punctata X-linked dominant type
Collagenous colitis
Connective tissue disease
Cystic fibrosis
Dermochondrocorneal dystrophy of François
Diabetes mellitus
Diastrophic dysplasia
DiGeorge syndrome
Dyggve-Melchior-Clausen dysplasia
Dysplasia epiphysealis hemimelica
Enchondromatosis
Familial fibrosing serositis
Familial idiopathic osteoarthropathy
Familial Mediterranean fever
Farber disease
Felty syndrome
Fetal alcohol syndrome
Fetal rubella infection
Fluorosis
Glycogen storage disease type 1
Gout
Hemochromatosis
Hemophilia
Henoch-Schönlein purpura
Hereditary multiple exostoses
Hydroxyapatite deposition disease
Hyperlipoproteinemia
Hypertrophic osteoarthropathy
Hypothyroidism
Infantile multisystem inflammatory disease
Inflammatory bowel disease
Intestinal bypass syndrome
Irritable hip syndrome
Jadassohn-Lewandowsky syndrome
Juvenile ankylosing spondylitis
Kashin-Beck disease
Kniest dysplasia
LAPS syndrome
Macrodystrophia lipomatosa
Melorheostosis
Membranous lipodystrophy
Mesomelic dysplasia Nievergelt type
Metatropic dysplasia
Mixed connective tissue disease
Mseleni joint disease
Muckle-Wells syndrome
Multicentric reticulohistiocytosis
Multiple epiphyseal dysplasia
Osebold-Remondini dysplasia
Osteogenesis imperfecta
Osteoglophonic dysplasia
Osteolysis without nephropathy
Osteopathia striata with cranial sclerosis
Osteoporosis-pseudoglioma syndrome
Otospondylomegaepiphyseal dysplasia
Paget disease of bone
Pancreatitis
Parastremmatic dysplasia
Parvovirus arthropathy
Plant thorn-induced syndrome
POEMS syndrome
Progressive pseudorheumatoid chondrodysplasia
Pseudoachondroplasia
Pseudodiastrophic dysplasia
Psoriatic arthritis
Pyle dysplasia
Reiter syndrome
Relapsing polychondritis
Rheumatoid arthritis
Sarcoidosis
Scleroderma
Secondary hyperparathyroidism
Sickle cell disease
Sjögren syndrome
Spondyloepimetaphyseal dysplasia Irapa type
Spondyloepimetaphyseal dysplasia Strudwick type
Spondyloepimetaphyseal dysplasia with joint laxity
Spondyloepiphyseal dysplasia congenita
Spondyloepiphyseal dysplasia tarda
Spondylometaphyseal dysplasia Kozlowski type
Sternocostoclavicular hyperostosis
Stickler syndrome
Thevenard syndrome
Trichorhinophalangeal dysplasia type 1
Trichorhinophalangeal dysplasia type 2
Weber-Christian syndrome
Wilson disease
Winchester syndrome
Wissler syndrome
Wolcott-Rallison syndrome
X-linked agammaglobulinemia
Y chromosome deletion
Acromegaly
Al-Aqeel Sewairi syndrome
Alkaptonuria
Amyloidosis
Ankylosing spondylitis
Anti-Jo-1 antibody syndrome
Arthropathy-camptodactyly syndrome
Autosomal dominant premature degenerative osteoarthropathy of the hip
Beekeeper arthropathy
Behçet disease
Blau syndrome
Blind loop syndrome
Calcium pyrophosphate dihydrate crystal deposition disease
Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
Caplan syndrome
Chondrodysplasia punctata Conradi-Hünermann type
Chondrodysplasia punctata X-linked dominant type
Collagenous colitis
Connective tissue disease
Cystic fibrosis
Dermochondrocorneal dystrophy of François
Diabetes mellitus
Diastrophic dysplasia
DiGeorge syndrome
Dyggve-Melchior-Clausen dysplasia
Dysplasia epiphysealis hemimelica
Enchondromatosis
Familial fibrosing serositis
Familial idiopathic osteoarthropathy
Familial Mediterranean fever
Farber disease
Felty syndrome
Fetal alcohol syndrome
Fetal rubella infection
Fluorosis
Glycogen storage disease type 1
Gout
Hemochromatosis
Hemophilia
Henoch-Schönlein purpura
Hereditary multiple exostoses
Hydroxyapatite deposition disease
Hyperlipoproteinemia
Hypertrophic osteoarthropathy
Hypothyroidism
Infantile multisystem inflammatory disease
Inflammatory bowel disease
Intestinal bypass syndrome
Irritable hip syndrome
Jadassohn-Lewandowsky syndrome
Juvenile ankylosing spondylitis
Kashin-Beck disease
Kniest dysplasia
LAPS syndrome
Macrodystrophia lipomatosa
Melorheostosis
Membranous lipodystrophy
Mesomelic dysplasia Nievergelt type
Metatropic dysplasia
Mixed connective tissue disease
Mseleni joint disease
Muckle-Wells syndrome
Multicentric reticulohistiocytosis
Multiple epiphyseal dysplasia
Osebold-Remondini dysplasia
Osteogenesis imperfecta
Osteoglophonic dysplasia
Osteolysis without nephropathy
Osteopathia striata with cranial sclerosis
Osteoporosis-pseudoglioma syndrome
Otospondylomegaepiphyseal dysplasia
Paget disease of bone
Pancreatitis
Parastremmatic dysplasia
Parvovirus arthropathy
Plant thorn-induced syndrome
POEMS syndrome
Progressive pseudorheumatoid chondrodysplasia
Pseudoachondroplasia
Pseudodiastrophic dysplasia
Psoriatic arthritis
Pyle dysplasia
Reiter syndrome
Relapsing polychondritis
Rheumatoid arthritis
Sarcoidosis
Scleroderma
Secondary hyperparathyroidism
Sickle cell disease
Sjögren syndrome
Spondyloepimetaphyseal dysplasia Irapa type
Spondyloepimetaphyseal dysplasia Strudwick type
Spondyloepimetaphyseal dysplasia with joint laxity
Spondyloepiphyseal dysplasia congenita
Spondyloepiphyseal dysplasia tarda
Spondylometaphyseal dysplasia Kozlowski type
Sternocostoclavicular hyperostosis
Stickler syndrome
Thevenard syndrome
Trichorhinophalangeal dysplasia type 1
Trichorhinophalangeal dysplasia type 2
Weber-Christian syndrome
Wilson disease
Winchester syndrome
Wissler syndrome
Wolcott-Rallison syndrome
X-linked agammaglobulinemia
Y chromosome deletion