Abnormality of the wrist

Symptom Information:

Symptom ID: HPO:0003019
Synonyms:
Abnormalities of the wrists [HPO:0003019]
Wrist anomaly [Orphanet:19720]
Wrist/carpal anomalies [Orphanet:19720]
Quality:
Cross references:
Orphanet:19720 "Wrist/carpal anomalies" [Orphanet:19720]
Is a (Direct Parents):
HPO         Abnormality of upper limb joint
Orphanet Upper limb segmental anomalies
Orphanet Abnormality of the carpal bones
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 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)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of upper limb joint(HPO:0009810)
                   Abnormality of the wrist(HPO:0003019)
MedDRA:
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)