Abnormality of the radius
Symptom Information:
Symptom ID: | HPO:0002818 | ||||||||
Synonyms: |
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Quality: | |||||||||
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 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: |
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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) |