Knee flexion contracture
Symptom Information:
Symptom ID: | HPO:0006380 | ||||||||||||||||||||
Synonyms: |
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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 lower limb(HPO:0002814) Abnormality of lower limb joint(HPO:0100491) Abnormality of the knee(HPO:0002815) Knee flexion contracture(HPO:0006380) Abnormal joint morphology(HPO:0001367) Abnormality of joint mobility(HPO:0011729) Flexion contracture(HPO:0001371) Limb joint contracture(HPO:0003121) Contractures of the joints of the lower limbs(HPO:0005750) Knee flexion contracture(HPO:0006380) Abnormality of lower limb joint(HPO:0100491) Abnormality of the knee(HPO:0002815) Knee flexion contracture(HPO:0006380) Abnormality of connective tissue(HPO:0003549) Flexion contracture(HPO:0001371) Limb joint contracture(HPO:0003121) Contractures of the joints of the lower limbs(HPO:0005750) Knee flexion contracture(HPO:0006380) Abnormality of the musculature(HPO:0003011) Abnormality of muscle morphology(HPO:0011805) Flexion contracture(HPO:0001371) Limb joint contracture(HPO:0003121) Contractures of the joints of the lower limbs(HPO:0005750) Knee flexion contracture(HPO:0006380) MedDRA: |
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Database Frequency: | 56 / 7739 | ||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED | (OMIM:300158) |
ARTHROGRYPOSIS, DISTAL, TYPE 1A | (OMIM:108120) |
ARTHROGRYPOSIS, DISTAL, TYPE 2A | (OMIM:193700) |
Argininemia | (Orphanet:90) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Autosomal dominant Emery-Dreifuss muscular dystrophy | (Orphanet:98853) |
Autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures | (Orphanet:363454) |
Autosomal dominant chondrodysplasia punctata | (Orphanet:79344) |
Autosomal dominant congenital benign spinal muscular atrophy | (Orphanet:1216) |
Autosomal dominant limb-girdle muscular dystrophy type 1B | (Orphanet:264) |
Autosomal dominant multiple pterygium syndrome | (Orphanet:65743) |
Autosomal recessive distal osteolysis syndrome | (Orphanet:2776) |
Autosomal recessive spastic paraplegia type 43 | (Orphanet:320370) |
Autosomal recessive spastic paraplegia type 45 | (Orphanet:320396) |
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA | (OMIM:609945) |
BRUCK SYNDROME 2 | (OMIM:609220) |
Bruck syndrome | (Orphanet:2771) |
CEREBROOCULOFACIOSKELETAL SYNDROME 1 | (OMIM:214150) |
CHROMOSOME 17p13.1 DELETION SYNDROME | (OMIM:613776) |
COFS syndrome | (Orphanet:1466) |
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTALDELAY | (OMIM:616266) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Congenital contractural arachnodactyly | (Orphanet:115) |
DPM1-CDG | (Orphanet:79322) |
Digitotalar dysmorphism | (Orphanet:1146) |
Fetal Gaucher disease | (Orphanet:85212) |
Freeman-Sheldon syndrome | (Orphanet:2053) |
Frontometaphyseal dysplasia | (Orphanet:1826) |
Gaucher disease type 2 | (Orphanet:77260) |
Genitopatellar syndrome | (Orphanet:85201) |
Gordon syndrome | (Orphanet:376) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Intellectual deficit - cataracts - calcified pinnae - myopathy | (Orphanet:3042) |
KAHRIZI SYNDROME | (OMIM:612713) |
KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT | (OMIM:148210) |
KID syndrome | (Orphanet:477) |
LETHAL CONGENITAL CONTRACTURE SYNDROME 7 | (OMIM:616286) |
Lenz-Majewski hyperostotic dwarfism | (Orphanet:2658) |
MENTAL RETARDATION, MICROCEPHALY, GROWTH RETARDATION, JOINT CONTRACTURES,AND FACIAL DYSMORPHISM | (OMIM:606242) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I | (OMIM:210710) |
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE III | (OMIM:210730) |
Macrocephaly - spastic paraplegia - dysmorphism | (Orphanet:2429) |
Marden-Walker syndrome | (Orphanet:2461) |
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus | (Orphanet:83473) |
Metaphyseal chondrodysplasia, Jansen type | (Orphanet:33067) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Muscular dystrophy, Selcen type | (Orphanet:199340) |
OTOONYCHOPERONEAL SYNDROME | (OMIM:259780) |
ROBERTS SYNDROME | (OMIM:268300) |
Roberts syndrome | (Orphanet:3103) |
SC PHOCOMELIA SYNDROME | (OMIM:269000) |
Spondyloepimetaphyseal dysplasia - short limb - abnormal calcification | (Orphanet:93358) |
Spondylometaphyseal dysplasia, Golden type | (Orphanet:168544) |
Stüve-Wiedemann syndrome | (Orphanet:3206) |
Van den Ende-Gupta syndrome | (Orphanet:2460) |
WHISTLING FACE SYNDROME, RECESSIVE FORM | (OMIM:277720) |