Genu recurvatum
Symptom Information:
Symptom ID: | HPO:0002816 | |||||||||||
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 joint morphology(HPO:0001367) Abnormality of lower limb joint(HPO:0100491) Abnormality of the knee(HPO:0002815) Genu recurvatum(HPO:0002816) 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) Genu recurvatum(HPO:0002816) MedDRA: Injury, poisoning and procedural complications(MedDRA:10022117) Bone and joint injuries(MedDRA:10005942) Limb injuries NEC (incl traumatic amputation)(MedDRA:10027686) Genu recurvatum(HPO:0002816) |
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Database Frequency: | 30 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
AARSKOG SYNDROME, AUTOSOMAL DOMINANT | (OMIM:100050) |
Aarskog-Scott syndrome | (Orphanet:915) |
Atkin-Flaitz syndrome | (Orphanet:1193) |
Autosomal recessive spastic paraplegia type 45 | (Orphanet:320396) |
CLARK-BARAITSER SYNDROME | (OMIM:300602) |
Cleft palate - short stature - vertebral anomalies | (Orphanet:2015) |
Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
De Barsy syndrome | (Orphanet:2962) |
Dermato-cardio-skeletal syndrome, Borrone type | (Orphanet:1266) |
Desbuquois syndrome | (Orphanet:1425) |
EHLERS-DANLOS SYNDROME, BEASLEY-COHEN TYPE | (OMIM:608763) |
Ehlers-Danlos syndrome type 1 | (Orphanet:90309) |
Ehlers-Danlos syndrome, cardiac valvular type | (Orphanet:230851) |
Goldblatt syndrome | (Orphanet:166272) |
Leri pleonosteosis | (Orphanet:2900) |
Linear nevus sebaceus syndrome | (Orphanet:2612) |
Linear verrucous nevus syndrome | (Orphanet:2611) |
MARFANOID HABITUS WITH SITUS INVERSUS | (OMIM:609008) |
MEIER-GORLIN SYNDROME 4 | (OMIM:613804) |
Marfan syndrome type 1 | (Orphanet:284963) |
Megalocornea-intellectual deficit syndrome | (Orphanet:2479) |
Metachromatic leukodystrophy | (Orphanet:512) |
Microspherophakia - metaphyseal dysplasia | (Orphanet:2551) |
Mucolipidosis type 4 | (Orphanet:578) |
Mulibrey nanism | (Orphanet:2576) |
Proteus-like syndrome | (Orphanet:2969) |
Pseudoachondroplasia | (Orphanet:750) |
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE | (OMIM:614066) |
Shprintzen-Goldberg syndrome | (Orphanet:2462) |
Spinocerebellar ataxia - dysmorphism | (Orphanet:1185) |