Abnormality of the radius

Symptom Information:

Symptom ID: HPO:0002818
Synonyms:
Radius anomaly [Orphanet:19240]
Congenital anomaly of radius (disorder) [Orphanet:19240]
Congenital anomaly of radius [Orphanet:19240]
Radius anomaly/absence/agenesis/hypoplasia/abnormal radial ray [Orphanet:19240]
Quality:
Cross references:
Orphanet:19240 "Radius anomaly/absence/agenesis/hypoplasia/abnormal radial ray" [Orphanet:19240]
UMLS:C1290460 "Congenital anomaly of radius" [Orphanet:19240]
Is a (Direct Parents):
Orphanet Upper limb segmental anomalies
HPO         Abnormal morphology of the radius
HPO         Osteosclerosis of the radius
HPO         Abnormality of the forearm
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 the forearm(HPO:0002973)
                         Abnormality of the radius(HPO:0002818)
MedDRA:
Database Frequency: 96 / 7739
Resource:

All diseases associated with this symptom:

46,XX disorder of sex development - anorectal anomalies (Orphanet:2973)
46,XX disorder of sex development - skeletal anomalies (Orphanet:2975)
Aase-Smith syndrome (Orphanet:916)
Acheiropodia (Orphanet:931)
Acro-pectoro-renal dysplasia (Orphanet:956)
Acro-renal-mandibular syndrome (Orphanet:958)
Acro-renal-ocular syndrome (Orphanet:959)
Acrodysostosis (Orphanet:950)
Acrofacial dysostosis, Rodriguez type (Orphanet:1788)
Acrorenal syndrome (Orphanet:971)
Adamantinoma (Orphanet:55881)
Amniotic bands (Orphanet:1034)
Antecubital pterygium syndrome (Orphanet:2987)
Arthrogryposis-like syndrome (Orphanet:1149)
Atrioventricular defect - blepharophimosis -radial defects (Orphanet:1352)
Auriculoosteodysplasia (Orphanet:114)
Autosomal recessive omodysplasia (Orphanet:93329)
Baller-Gerold syndrome (Orphanet:1225)
Boomerang dysplasia (Orphanet:1263)
Bowed tibiae - radial anomalies - osteopenia - fractures (Orphanet:3331)
Brachydactyly - elbow wrist dysplasia (Orphanet:1275)
Camurati-Engelmann disease (Orphanet:1328)
Cantrell pentalogy (Orphanet:1335)
Cenani-Lenz syndrome (Orphanet:3258)
Diabetic embryopathy (Orphanet:1926)
Diaphragmatic defect - limb deficiency - skull defect (Orphanet:2141)
Distal limb deficiencies - micrognathia syndrome (Orphanet:1307)
Duane retraction syndrome (Orphanet:233)
Dyschondrosteosis - nephritis (Orphanet:1765)
Eye defects - arachnodactyly - cardiopathy (Orphanet:2725)
Fanconi anemia (Orphanet:84)
Femur-fibula-ulna complex (Orphanet:2019)
Fibular aplasia - complex brachydactyly (Orphanet:2639)
Hartsfield-Bixler-Demyer syndrome (Orphanet:2117)
Heart-hand syndrome type 2 (Orphanet:1350)
Holoprosencephaly - caudal dysgenesis (Orphanet:2165)
Holoprosencephaly - radial heart renal anomalies (Orphanet:3186)
Holt-Oram syndrome (Orphanet:392)
Hurler-Scheie syndrome (Orphanet:93476)
Hypertryptophanemia (Orphanet:2224)
IVIC syndrome (Orphanet:2307)
Juberg-Hayward syndrome (Orphanet:2319)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Laurin-Sandrow syndrome (Orphanet:2378)
Lethal faciocardiomelic dysplasia (Orphanet:1972)
Lowry-Wood syndrome (Orphanet:1824)
Léri-Weill dyschondrosteosis (Orphanet:240)
Madelung deformity (Orphanet:35688)
Medeira-Dennis-Donnai syndrome (Orphanet:2476)
Mesomelic dwarfism, Nievergelt type (Orphanet:2633)
Mesomelic dwarfism, Reinhardt-Pfeiffer type (Orphanet:2634)
Metaphyseal anadysplasia (Orphanet:1040)
Microgastria - limb reduction defect (Orphanet:2538)
Mietens syndrome (Orphanet:2557)
Moebius syndrome (Orphanet:570)
Multiple osteochondromas (Orphanet:321)
Nager syndrome (Orphanet:245)
Neurogenic arthrogryposis multiplex congenita (Orphanet:1143)
Oculoauriculovertebral spectrum with radial defects (Orphanet:2549)
Omodysplasia (Orphanet:2733)
Ophthalmomandibulomelic dysplasia (Orphanet:2741)
Orofaciodigital syndrome type 10 (Orphanet:2756)
Phocomelia - ectrodactyly - deafness - sinus arrhythmia (Orphanet:2878)
Phocomelia, Schinzel type (Orphanet:2879)
Poland syndrome (Orphanet:2911)
Postaxial acrofacial dysostosis (Orphanet:246)
RAPADILINO syndrome (Orphanet:3021)
Radial hypoplasia - triphalangeal thumbs - hypospadias - maxillary diastema (Orphanet:2252)
Radial ray hypoplasia - choanal atresia (Orphanet:3026)
Radio-renal syndrome (Orphanet:3015)
Radius absent - anogenital anomalies (Orphanet:3016)
Richieri Costa-Pereira syndrome (Orphanet:3102)
Ring chromosome 4 (Orphanet:1447)
Roberts syndrome (Orphanet:3103)
Rothmund-Thomson syndrome (Orphanet:2909)
Rothmund-Thomson syndrome type 2 (Orphanet:221016)
Sheldon-Hall syndrome (Orphanet:1147)
Shoulder and thorax deformity - congenital heart disease (Orphanet:1940)
Sirenomelia (Orphanet:3169)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Split hand - urinary anomalies - spina bifida (Orphanet:2437)
Symbrachydactyly of hands and feet (Orphanet:1570)
Syndactyly - telecanthus - anogenital and renal malformations (Orphanet:140952)
Thrombocytopenia - absent radius (Orphanet:3320)
Tricho-dento-osseous syndrome (Orphanet:3352)
Ulbright-Hodes syndrome (Orphanet:3404)
Ulna hypoplasia - intellectual deficit (Orphanet:2249)
Ulna metaphyseal dysplasia syndrome (Orphanet:1837)
Ulnar hypoplasia - split foot (Orphanet:1122)
Ulnar-mammary syndrome (Orphanet:3138)
Upper limb mesomelic dysplasia (Orphanet:2497)
VACTERL with hydrocephalus (Orphanet:3412)
VACTERL/VATER association (Orphanet:887)
Von Voss-Cherstvoy syndrome (Orphanet:3439)
Weismann-Netter syndrome (Orphanet:3344)
XK aprosencephaly (Orphanet:3469)