Limited elbow extension
Symptom Information:
Symptom ID: | HPO:0001377 | |||||||||||||
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 joint morphology(HPO:0001367) Abnormality of joint mobility(HPO:0011729) Limitation of joint mobility(HPO:0001376) Limited elbow movement(HPO:0002996) Limited elbow extension(HPO:0001377) Abnormality of upper limb joint(HPO:0009810) Abnormality of the elbow(HPO:0009811) Limited elbow movement(HPO:0002996) Limited elbow extension(HPO:0001377) 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) MedDRA: |
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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) |