Genu recurvatum

Symptom Information:

Symptom ID: HPO:0002816
Synonyms:
Genu recurvata [HPO:0002816]
Hyperextension deformity of knee (disorder) [Orphanet:21520]
Genu recurvata [OMIM:Genu recurvata]
Genu recurvatum [OMIM:Genu recurvatum]
Genu recurvatum [Orphanet:21520]
Joint hyperextension [MedDRA:10062310]
Genu recurvatum [MedDRA:10062310]
Hyperextension of knee [MedDRA:10062310]
Limb hyperextension [MedDRA:10062310]
Genu recurvatum (1 family) [OMIM:Genu recurvatum (1 family)]
Genu recurvatum (in some patients) [OMIM:Genu recurvatum (in some patients)]
Quality:
Cross references:
Orphanet:21520 "Genu recurvatum" [Orphanet:21520]
OMIM: "Genu recurvata" [OMIM:Genu recurvata]
OMIM: "Genu recurvatum" [OMIM:Genu recurvatum]
OMIM: "Genu recurvatum (1 family)" [OMIM:Genu recurvatum (1 family)]
OMIM: "Genu recurvatum (in some patients)" [OMIM:Genu recurvatum (in some patients)]
Is a (Direct Parents):
Orphanet Abnormality of the knee
MedDRA Limb injuries NEC (incl traumatic amputation)
HPO         Abnormality of the knee
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)
                            Genu recurvatum(HPO:0002816)
             Abnormal joint morphology(HPO:0001367)
                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)
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)