Abnormal joint morphology
Symptom Information:
| Symptom ID: | HPO:0001367 | ||||
| Synonyms: |
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| Cross references: |
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| 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) MedDRA: |
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| Database Frequency: | 53 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| AGONADISM, 46,XY, WITH MENTAL RETARDATION, SHORT STATURE, RETARDEDBONE AGE, AND MULTIPLE EXTRAGENITAL MALFORMATIONS | (OMIM:600908) |
| Albright hereditary osteodystrophy | (Orphanet:665) |
| Alkaptonuria | (Orphanet:56) |
| Autosomal dominant spastic paraplegia type 31 | (Orphanet:101011) |
| Bowen-Conradi syndrome | (Orphanet:1270) |
| Brachydactyly-long thumb syndrome | (Orphanet:2946) |
| CINCA syndrome | (Orphanet:1451) |
| CORACOCLAVICULAR JOINT, ANOMALOUS | (OMIM:121350) |
| Cerebrotendinous xanthomatosis | (Orphanet:909) |
| Dysspondyloenchondromatosis | (Orphanet:85198) |
| Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
| Familial articular chondrocalcinosis | (Orphanet:1416) |
| Farber lipogranulomatosis | (Orphanet:333) |
| Felty syndrome | (Orphanet:47612) |
| Gaucher disease | (Orphanet:355) |
| Glutaryl-CoA dehydrogenase deficiency | (Orphanet:25) |
| Greenberg dysplasia | (Orphanet:1426) |
| Hereditary arterial and articular multiple calcification syndrome | (Orphanet:289601) |
| Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
| Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
| Intellectual deficit - balding - patella luxation - acromicria | (Orphanet:3041) |
| Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
| Juvenile idiopathic arthritis | (Orphanet:92) |
| Juvenile rheumatoid factor-negative polyarthritis | (Orphanet:85408) |
| Juvenile rheumatoid factor-positive polyarthritis | (Orphanet:85435) |
| Keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome | (Orphanet:281201) |
| Kniest dysplasia | (Orphanet:485) |
| Laron syndrome | (Orphanet:633) |
| Legg-Calvé-Perthes disease | (Orphanet:2380) |
| Madelung deformity | (Orphanet:35688) |
| Maffucci syndrome | (Orphanet:163634) |
| Marfan syndrome | (Orphanet:558) |
| Metachondromatosis | (Orphanet:2499) |
| Metaphyseal acroscyphodysplasia | (Orphanet:1240) |
| Multiple epiphyseal dysplasia due to collagen 9 anomaly | (Orphanet:166002) |
| Multiple epiphyseal dysplasia type 1 | (Orphanet:93308) |
| Multiple epiphyseal dysplasia type 4 | (Orphanet:93307) |
| Multiple epiphyseal dysplasia type 5 | (Orphanet:93311) |
| Multiple epiphyseal dysplasia, Al-Gazali type | (Orphanet:166024) |
| OSTEOGENESIS IMPERFECTA WITH OPALESCENT TEETH, BLUE SCLERAE AND WORMIANBONES, BUT WITHOUT FRACTURES | (OMIM:166230) |
| Pantothenate kinase-associated neurodegeneration | (Orphanet:157850) |
| Progeria - short stature - pigmented nevi | (Orphanet:2959) |
| Recessive dystrophic epidermolysis bullosa inversa | (Orphanet:79409) |
| SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 2 | (OMIM:183840) |
| Scleroderma | (Orphanet:801) |
| Spondyloepimetaphyseal dysplasia, Irapa type | (Orphanet:93351) |
| Spondylometaphyseal dysplasia, Kozlowski type | (Orphanet:93314) |
| Spondylometaphyseal dysplasia, Schmidt type | (Orphanet:93316) |
| Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence | (Orphanet:3201) |
| Von Voss-Cherstvoy syndrome | (Orphanet:3439) |
| Wilson disease | (Orphanet:905) |
| X-linked dominant chondrodysplasia punctata | (Orphanet:35173) |
| X-linked hypophosphatemia | (Orphanet:89936) |