Abnormality of the ulna
Symptom Information:
Symptom ID: | HPO:0002997 | ||||||
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 ulna(HPO:0002997) MedDRA: |
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Database Frequency: | 75 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
2q31.1 microdeletion syndrome | (Orphanet:251014) |
3M syndrome | (Orphanet:2616) |
Absent thumb - short stature - immunodeficiency | (Orphanet:2951) |
Absent tibia - polydactyly - arachnoid cyst | (Orphanet:3328) |
Acheiropodia | (Orphanet:931) |
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) |
Alagille syndrome | (Orphanet:52) |
Antecubital pterygium syndrome | (Orphanet:2987) |
Aspartylglucosaminuria | (Orphanet:93) |
Atrioventricular defect - blepharophimosis -radial defects | (Orphanet:1352) |
Blepharophimosis - radioulnar synostosis | (Orphanet:1256) |
Boomerang dysplasia | (Orphanet:1263) |
Brachydactyly - elbow wrist dysplasia | (Orphanet:1275) |
Brachydactyly type A1 | (Orphanet:93388) |
Camurati-Engelmann disease | (Orphanet:1328) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Cenani-Lenz syndrome | (Orphanet:3258) |
Cornelia de Lange syndrome | (Orphanet:199) |
Diaphragmatic defect - limb deficiency - skull defect | (Orphanet:2141) |
Distal limb deficiencies - micrognathia syndrome | (Orphanet:1307) |
Dyschondrosteosis - nephritis | (Orphanet:1765) |
Dysspondyloenchondromatosis | (Orphanet:85198) |
Fanconi anemia | (Orphanet:84) |
Femur-fibula-ulna complex | (Orphanet:2019) |
Fibular aplasia - complex brachydactyly | (Orphanet:2639) |
Fibular aplasia - ectrodactyly | (Orphanet:1118) |
Fibulo-ulnar hypoplasia - renal anomalies | (Orphanet:2256) |
Gollop-Wolfgang complex | (Orphanet:1986) |
Heart-hand syndrome type 2 | (Orphanet:1350) |
Holoprosencephaly - radial heart renal anomalies | (Orphanet:3186) |
Holzgreve-Wagner-Rehder syndrome | (Orphanet:2167) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hypertryptophanemia | (Orphanet:2224) |
Hypogonadism - mitral valve prolapse - intellectual deficit | (Orphanet:2233) |
Langer mesomelic dysplasia | (Orphanet:2632) |
Lethal faciocardiomelic dysplasia | (Orphanet:1972) |
Léri-Weill dyschondrosteosis | (Orphanet:240) |
Madelung deformity | (Orphanet:35688) |
Mesomelic dwarfism, Nievergelt type | (Orphanet:2633) |
Mesomelic dwarfism, Reinhardt-Pfeiffer type | (Orphanet:2634) |
Mesomelic dysplasia, Savarirayan type | (Orphanet:85170) |
Metaphyseal anadysplasia | (Orphanet:1040) |
Microgastria - limb reduction defect | (Orphanet:2538) |
Mietens syndrome | (Orphanet:2557) |
Moebius syndrome | (Orphanet:570) |
Mullerian duct anomalies - limb anomalies | (Orphanet:2491) |
Multiple epiphyseal dysplasia | (Orphanet:251) |
Multiple osteochondromas | (Orphanet:321) |
Ophthalmomandibulomelic dysplasia | (Orphanet:2741) |
Phocomelia - ectrodactyly - deafness - sinus arrhythmia | (Orphanet:2878) |
Phocomelia, Schinzel type | (Orphanet:2879) |
Poland syndrome | (Orphanet:2911) |
Postaxial acrofacial dysostosis | (Orphanet:246) |
Ring chromosome 4 | (Orphanet:1447) |
Robin sequence - oligodactyly | (Orphanet:3104) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Spondyloperipheral dysplasia - short ulna | (Orphanet:1856) |
Symbrachydactyly of hands and feet | (Orphanet:1570) |
Thalidomide embryopathy | (Orphanet:3312) |
Thrombocytopenia - absent radius | (Orphanet:3320) |
Tibial aplasia - ectrodactyly | (Orphanet:3329) |
Tricho-dento-osseous syndrome | (Orphanet:3352) |
Ulbright-Hodes syndrome | (Orphanet:3404) |
Ulna hypoplasia - intellectual deficit | (Orphanet:2249) |
Ulna metaphyseal dysplasia syndrome | (Orphanet:1837) |
Ulnar-mammary syndrome | (Orphanet:3138) |
Ulnar/fibula ray defect - brachydactyly | (Orphanet:52056) |
Upper limb mesomelic dysplasia | (Orphanet:2497) |
Von Voss-Cherstvoy syndrome | (Orphanet:3439) |
WT limb-blood syndrome | (Orphanet:3466) |
Weismann-Netter syndrome | (Orphanet:3344) |