Abnormality of the humerus

Symptom Information:

Symptom ID: HPO:0003063
Synonyms:
Abnormality of the humeri [HPO:0003063]
Humerus anomaly [Orphanet:19180]
Congenital anomaly of humerus (disorder) [Orphanet:19180]
Congenital anomaly of humerus [Orphanet:19180]
Humerus anomaly/absence/agenesis/hypoplasia/congenital humerus varus [Orphanet:19180]
Quality:
Cross references:
Orphanet:19180 "Humerus anomaly/absence/agenesis/hypoplasia/congenital humerus varus" [Orphanet:19180]
UMLS:C1290458 "Congenital anomaly of humerus" [Orphanet:19180]
Is a (Direct Parents):
Orphanet Upper limb segmental anomalies
HPO         Abnormal humeral ossification
HPO         Abnormality of the upper arm
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 upper arm(HPO:0001454)
                         Abnormality of the humerus(HPO:0003063)
MedDRA:
Database Frequency: 36 / 7739
Resource:

All diseases associated with this symptom:

Acheiropodia (Orphanet:931)
Acro-renal-ocular syndrome (Orphanet:959)
Adamantinoma (Orphanet:55881)
Autosomal dominant omodysplasia (Orphanet:93328)
Autosomal recessive omodysplasia (Orphanet:93329)
Boomerang dysplasia (Orphanet:1263)
Brachydactyly - elbow wrist dysplasia (Orphanet:1275)
Camurati-Engelmann disease (Orphanet:1328)
Diaphragmatic defect - limb deficiency - skull defect (Orphanet:2141)
Heart-hand syndrome type 2 (Orphanet:1350)
Holoprosencephaly - radial heart renal anomalies (Orphanet:3186)
Holt-Oram syndrome (Orphanet:392)
Humerus trochlea aplasia (Orphanet:3383)
Léri-Weill dyschondrosteosis (Orphanet:240)
Mesomelia-synostoses syndrome (Orphanet:2496)
Mesomelic dysplasia, Kantaputra type (Orphanet:1836)
Metaphyseal dysplasia - maxillary hypoplasia - brachydacty (Orphanet:2504)
Microgastria - limb reduction defect (Orphanet:2538)
Mullerian duct anomalies - limb anomalies (Orphanet:2491)
Multiple osteochondromas (Orphanet:321)
Occipital horn syndrome (Orphanet:198)
Oculomaxillofacial dysostosis (Orphanet:1794)
Omodysplasia (Orphanet:2733)
Ophthalmomandibulomelic dysplasia (Orphanet:2741)
Phocomelia - ectrodactyly - deafness - sinus arrhythmia (Orphanet:2878)
Phocomelia, Schinzel type (Orphanet:2879)
Poland syndrome (Orphanet:2911)
Rhizomelic dysplasia, Patterson-Lowry type (Orphanet:2831)
Rhizomelic syndrome, Urbach type (Orphanet:3098)
Satoyoshi syndrome (Orphanet:3130)
Shoulder and thorax deformity - congenital heart disease (Orphanet:1940)
Symbrachydactyly of hands and feet (Orphanet:1570)
Thalidomide embryopathy (Orphanet:3312)
Thrombocytopenia - absent radius (Orphanet:3320)
Ulnar-mammary syndrome (Orphanet:3138)
Weismann-Netter syndrome (Orphanet:3344)