Limited elbow extension

Symptom Information:

Symptom ID: HPO:0001377
Synonyms:
Decreased elbow extension [HPO:0001377]
Elbow limited extension [HPO:0001377]
Limitation of elbow extension [HPO:0001377]
Limited extension at elbows [HPO:0001377]
Limited forearm extension [HPO:0001377]
Restricted elbow extension [HPO:0001377]
Elbow limited extension [OMIM:Elbow limited extension]
Limitation of elbow extension [OMIM:Limitation of elbow extension]
Limited elbow extension [OMIM:Limited elbow extension]
Limited extension at elbows [OMIM:Limited extension at elbows]
Limited forearm extension [OMIM:Limited forearm extension]
Restricted elbow extension [OMIM:Restricted elbow extension]
Decreased elbow extension (in some patients) [OMIM:Decreased elbow extension (in some patients)]
Quality:
Cross references:
OMIM: "Elbow limited extension" [OMIM:Elbow limited extension]
OMIM: "Limitation of elbow extension" [OMIM:Limitation of elbow extension]
OMIM: "Limited elbow extension" [OMIM:Limited elbow extension]
OMIM: "Limited extension at elbows" [OMIM:Limited extension at elbows]
OMIM: "Limited forearm extension" [OMIM:Limited forearm extension]
OMIM: "Restricted elbow extension" [OMIM:Restricted elbow extension]
OMIM: "Decreased elbow extension (in some patients)" [OMIM:Decreased elbow extension (in some patients)]
Is a (Direct Parents):
HPO         Limited elbow movement
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)
                            Limited elbow movement(HPO:0002996)
                               Limited elbow extension(HPO:0001377)
             Abnormal joint morphology(HPO:0001367)
                Abnormality of upper limb joint(HPO:0009810)
                   Abnormality of the elbow(HPO:0009811)
                      Limited elbow movement(HPO:0002996)
                         Limited elbow extension(HPO:0001377)
                Abnormality of joint mobility(HPO:0011729)
                   Limitation of joint mobility(HPO:0001376)
                      Limited elbow movement(HPO:0002996)
                         Limited elbow extension(HPO:0001377)
MedDRA:
Database Frequency: 38 / 7739
Resource:

All diseases associated with this symptom:

Achondroplasia (Orphanet:15)
Acromesomelic dysplasia, Maroteaux type (Orphanet:40)
Antecubital pterygium syndrome (Orphanet:2987)
Autosomal recessive omodysplasia (Orphanet:93329)
COLD-INDUCED SWEATING SYNDROME 2 (OMIM:610313)
CORNELIA DE LANGE SYNDROME 1 (OMIM:122470)
CORNELIA DE LANGE SYNDROME 5 (OMIM:300882)
Cartilage-hair hypoplasia (Orphanet:175)
Cold-induced sweating syndrome (Orphanet:157820)
Cornelia de Lange syndrome (Orphanet:199)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Distal monosomy 10q (Orphanet:96148)
Hypertryptophanemia (Orphanet:2224)
Hypochondroplasia (Orphanet:429)
Intellectual deficit, X-linked, Turner type (Orphanet:85328)
Juberg-Hayward syndrome (Orphanet:2319)
Metaphyseal anadysplasia (Orphanet:1040)
Metaphyseal chondrodysplasia, Kaitila type (Orphanet:166038)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Nager syndrome (Orphanet:245)
Nail-patella syndrome (Orphanet:2614)
Occipital horn syndrome (Orphanet:198)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Otopalatodigital syndrome type 1 (Orphanet:90650)
Primordial short stature - microdontia - opalescent and rootless teeth (Orphanet:46658)
Proximal radioulnar synostosis (Orphanet:3269)
Pseudoachondroplasia (Orphanet:750)
Pyle disease (Orphanet:3005)
RADIAL HEADS, POSTERIOR DISLOCATION OF (OMIM:179200)
Ruvalcaba syndrome (Orphanet:3121)
SPONASTRIME dysplasia (Orphanet:93357)
Spondyloepimetaphyseal dysplasia, Irapa type (Orphanet:93351)
Spondyloepimetaphyseal dysplasia, Missouri type (Orphanet:93356)
Spondyloepimetaphyseal dysplasia, matrilin-3 type (Orphanet:156728)
Spondyloperipheral dysplasia - short ulna (Orphanet:1856)
Suarez-Stickler syndrome (Orphanet:166277)
Weaver syndrome (Orphanet:3447)
X-linked spondyloepimetaphyseal dysplasia (Orphanet:93349)