Abnormality of the ulna

Symptom Information:

Symptom ID: HPO:0002997
Ulna anomaly [Orphanet:19300]
Congenital anomaly of ulna (disorder) [Orphanet:19300]
Congenital anomaly of ulna [Orphanet:19300]
Ulnar/cubital anomaly/absence/agenesis/hypoplasia/abnormal ulnar/cubital ray [Orphanet:19300]
Cross references:
Orphanet:19300 "Ulnar/cubital anomaly/absence/agenesis/hypoplasia/abnormal ulnar/cubital ray" [Orphanet:19300]
UMLS:C1290461 "Congenital anomaly of ulna" [Orphanet:19300]
Is a (Direct Parents):
HPO         Abnormal morphology of ulna
Orphanet Upper limb segmental anomalies
HPO         Abnormality of the forearm
Is a (Whole tree): HPO:
    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)
Database Frequency: 75 / 7739

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)