Abnormality of the wrist
Symptom Information:
Symptom ID: | HPO:0003019 | ||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) Abnormality of upper limb joint(HPO:0009810) Abnormality of the wrist(HPO:0003019) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the upper limb(HPO:0002817) Abnormality of upper limb joint(HPO:0009810) Abnormality of the wrist(HPO:0003019) MedDRA: |
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Database Frequency: | 52 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
Absent thumb - short stature - immunodeficiency | (Orphanet:2951) |
Acromesomelic dysplasia, Hunter-Thomson type | (Orphanet:968) |
Arthrogryposis multiplex congenita | (Orphanet:1037) |
Auriculoosteodysplasia | (Orphanet:114) |
Autosomal dominant Larsen syndrome | (Orphanet:503) |
Baller-Gerold syndrome | (Orphanet:1225) |
Brachydactylous dwarfism, Mseleni type | (Orphanet:2619) |
Carpotarsal osteochondromatosis | (Orphanet:2767) |
Cleft palate - stapes fixation - oligodontia | (Orphanet:2010) |
Craniofacial-deafness-hand syndrome | (Orphanet:1529) |
Dent disease type 1 | (Orphanet:93622) |
Dermatoosteolysis, Kirghizian type | (Orphanet:1657) |
Distal limb deficiencies - micrognathia syndrome | (Orphanet:1307) |
Dyggve-Melchior-Clausen disease | (Orphanet:239) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Ellis Van Creveld syndrome | (Orphanet:289) |
Epiphyseal dysplasia - hearing loss - dysmorphism | (Orphanet:1825) |
Heart-hand syndrome type 2 | (Orphanet:1350) |
Holt-Oram syndrome | (Orphanet:392) |
Humero-radial synostosis | (Orphanet:3265) |
Humerus trochlea aplasia | (Orphanet:3383) |
Hypertryptophanemia | (Orphanet:2224) |
Hypophosphatemic rickets, autosomal recessive, 2 | (OMIM:613312) |
Juberg-Hayward syndrome | (Orphanet:2319) |
Kienbock disease | (Orphanet:97332) |
Langer mesomelic dysplasia | (Orphanet:2632) |
Laurin-Sandrow syndrome | (Orphanet:2378) |
Léri-Weill dyschondrosteosis | (Orphanet:240) |
Madelung deformity | (Orphanet:35688) |
Mesomelia-synostoses syndrome | (Orphanet:2496) |
Mesomelic dwarfism, Nievergelt type | (Orphanet:2633) |
Microbrachycephaly - ptosis - cleft lip | (Orphanet:2511) |
Mucolipidosis type 2 | (Orphanet:576) |
Mullerian duct anomalies - limb anomalies | (Orphanet:2491) |
Multicentric carpo-tarsal osteolysis with or without nephropathy | (Orphanet:2774) |
Multiple epiphyseal dysplasia | (Orphanet:251) |
Occipital horn syndrome | (Orphanet:198) |
Phocomelia - ectrodactyly - deafness - sinus arrhythmia | (Orphanet:2878) |
Proteus syndrome | (Orphanet:744) |
Proximal symphalangism | (Orphanet:3250) |
Pseudoachondroplasia | (Orphanet:750) |
Radial ray hypoplasia - choanal atresia | (Orphanet:3026) |
Satoyoshi syndrome | (Orphanet:3130) |
Sheldon-Hall syndrome | (Orphanet:1147) |
Shoulder and thorax deformity - congenital heart disease | (Orphanet:1940) |
Splenogonadal fusion - limb defects - micrognathia | (Orphanet:2063) |
Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
Spondyloepimetaphyseal dysplasia, Irapa type | (Orphanet:93351) |
Spondylometaphyseal dysplasia, 'corner fracture' type | (Orphanet:93315) |
Torg-Winchester syndrome | (Orphanet:3460) |
Ulnar-mammary syndrome | (Orphanet:3138) |
WT limb-blood syndrome | (Orphanet:3466) |