Abnormality of the humerus
Symptom Information:
Symptom ID: | HPO:0003063 | ||||||
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 upper arm(HPO:0001454) Abnormality of the humerus(HPO:0003063) MedDRA: |
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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) |