Abnormality of the elbow

Symptom Information:

Symptom ID: HPO:0009811
Synonyms:
Abnormality of the elbows [HPO:0009811]
Elbow anomaly [Orphanet:19420]
Elbow anomalies(excluding luxation) [Orphanet:19420]
Quality:
Cross references:
Orphanet:19420 "Elbow anomalies(excluding luxation)" [Orphanet:19420]
Is a (Direct Parents):
HPO         Abnormality of upper limb joint
Orphanet Upper limb segmental anomalies
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 joint morphology(HPO:0001367)
                Abnormality of upper limb joint(HPO:0009810)
                   Abnormality of the elbow(HPO:0009811)
             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)
MedDRA:
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)