Abnormality of the elbow
Symptom Information:
| Symptom ID: | HPO:0009811 | ||||
| Synonyms: |
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| 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 upper limb joint(HPO:0009810) Abnormality of the elbow(HPO:0009811) Abnormal joint morphology(HPO:0001367) Abnormality of upper limb joint(HPO:0009810) Abnormality of the elbow(HPO:0009811) MedDRA: |
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| Database Frequency: | 30 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| 3M syndrome | (Orphanet:2616) |
| Achondroplasia | (Orphanet:15) |
| Alopecia - contractures - dwarfism - intellectual deficit | (Orphanet:1005) |
| Antecubital pterygium syndrome | (Orphanet:2987) |
| Bone dysplasia, lethal Holmgren type | (Orphanet:1842) |
| Brachydactylous dwarfism, Mseleni type | (Orphanet:2619) |
| Distal monosomy 10p | (Orphanet:1580) |
| Ehlers-Danlos syndrome type 11 | (Orphanet:2295) |
| Femur-fibula-ulna complex | (Orphanet:2019) |
| Heart-hand syndrome type 2 | (Orphanet:1350) |
| Hirsutism - skeletal dysplasia - intellectual deficit | (Orphanet:2156) |
| Hurler syndrome | (Orphanet:93473) |
| Hypertrichosis cubiti - short stature | (Orphanet:2220) |
| Hypertryptophanemia | (Orphanet:2224) |
| Hypochondroplasia | (Orphanet:429) |
| Intellectual deficit - microcephaly - phalangeal - facial abnormalities | (Orphanet:3067) |
| Intellectual deficit, X-linked, Armfield type | (Orphanet:85276) |
| Juberg-Hayward syndrome | (Orphanet:2319) |
| Laron syndrome | (Orphanet:633) |
| Lethal congenital contracture syndrome type 1 | (Orphanet:1486) |
| Madelung deformity | (Orphanet:35688) |
| Mullerian duct anomalies - limb anomalies | (Orphanet:2491) |
| Nail-patella syndrome | (Orphanet:2614) |
| Neurofaciodigitorenal syndrome | (Orphanet:2673) |
| Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
| Pyle disease | (Orphanet:3005) |
| Radio-renal syndrome | (Orphanet:3015) |
| Rhizomelic syndrome, Urbach type | (Orphanet:3098) |
| Ruvalcaba syndrome | (Orphanet:3121) |
| Synostosis - microcephaly - scoliosis | (Orphanet:3268) |