Abnormality of the knee
Symptom Information:
Symptom ID: | HPO:0002815 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
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) Abnormal joint morphology(HPO:0001367) Abnormality of lower limb joint(HPO:0100491) Abnormality of the knee(HPO:0002815) MedDRA: |
||||
Database Frequency: | 19 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Axial mesodermal dysplasia spectrum | (Orphanet:1834) |
Brachydactylous dwarfism, Mseleni type | (Orphanet:2619) |
Coxo-podo-patellar syndrome | (Orphanet:1509) |
Cranio-osteoarthropathy | (Orphanet:1525) |
Cyprus facial-neuromusculoskeletal syndrome | (Orphanet:2674) |
Dislocation of the hip - dysmorphism | (Orphanet:2412) |
EPIPHYSEAL DYSPLASIA, MULTIPLE, 6 | (OMIM:614135) |
Ehlers-Danlos syndrome type 11 | (Orphanet:2295) |
Genochondromatosis type 1 | (Orphanet:85197) |
Hemimelia | (Orphanet:2130) |
Hereditary sensory and autonomic neuropathy type 2 | (Orphanet:970) |
Hypertryptophanemia | (Orphanet:2224) |
Mesomelia-synostoses syndrome | (Orphanet:2496) |
POPLITEAL CYST | (OMIM:175750) |
Progressive pseudorheumatoid arthropathy of childhood | (Orphanet:1159) |
Rhizomelic syndrome, Urbach type | (Orphanet:3098) |
Satoyoshi syndrome | (Orphanet:3130) |
Splenogonadal fusion - limb defects - micrognathia | (Orphanet:2063) |
Trochlear dysplasia | (Orphanet:1863) |