Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Lethal congenital contracture syndrome type 2 (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Lethal congenital contracture syndrome type 3 (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Foot joint - range of movement |
Is a |
True |
Range of joint movement |
Inferred relationship |
Some |
|
Hand joint range of movement (observable entity) |
Is a |
True |
Range of joint movement |
Inferred relationship |
Some |
|
Inherited arthrogryposis |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Malignant hyperthermia with arthrogryposis and torticollis syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
4 |
X-linked lethal multiple pterygium syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Lethal congenital contracture syndrome type 5 |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Contracture with ectodermal dysplasia and orofacial cleft syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
7 |
Neurogenic arthrogryposis multiplex congenita (disorder) |
Interprets |
False |
Range of joint movement |
Inferred relationship |
Some |
2 |
Autosomal dominant multiple pterygium syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Distal arthrogryposis type 5D (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Joint contracture, webbed neck, micrognathia, hypoplastic nipple syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
5 |
Larsen-like syndrome B3GAT3 type |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
4 |
Congenital neuropathy with arthrogryposis multiplex congenita |
Interprets |
False |
Range of joint movement |
Inferred relationship |
Some |
3 |
Arthrogryposis with renal dysfunction and cholestasis syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Camptodactyly with joint contracture and facial skeletal defect syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Camptobrachydactyly (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
4 |
Autism spectrum disorder, epilepsy, arthrogryposis syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Contracture of joint |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Distal arthrogryposis type 1 (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Neurogenic arthrogryposis multiplex congenita (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
4 |
On examination - reduced joint movement |
Interprets |
False |
Range of joint movement |
Inferred relationship |
Some |
4 |
On examination - reduced movement of spine |
Interprets |
False |
Range of joint movement |
Inferred relationship |
Some |
2 |
On examination - reduced movement of arm |
Interprets |
False |
Range of joint movement |
Inferred relationship |
Some |
2 |
Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
4 |
Contracture of multiple joints |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
German syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
1 |
Contracture of joint following injury (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Lethal congenital contracture syndrome type 1 (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Congenital arthrogryposis caused by teratogen (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
On examination - reduced movement of wrist |
Interprets |
False |
Range of joint movement |
Inferred relationship |
Some |
2 |
Hydrocephalus with cleft palate and joint contracture syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
9 |
Distal arthrogryposis syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Temporomandibular joint stiff |
Interprets |
False |
Range of joint movement |
Inferred relationship |
Some |
1 |
Arthrogryposis and ectodermal dysplasia syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
6 |
Arthrogryposis with renal dysfunction and cholestasis syndrome (disorder) |
Interprets |
False |
Range of joint movement |
Inferred relationship |
Some |
4 |
Kuskokwim syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Congenital contractural arachnodactyly |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Multiple stiff joints |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
1 |
Morning stiffness - joint |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
1 |
Marfanoid joint hypermobility syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Hypermobility of joint |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
1 |
Spondyloepimetaphyseal dysplasia with joint laxity |
Interprets |
False |
Range of joint movement |
Inferred relationship |
Some |
4 |
Distal arthrogryposis type 3 (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Prenatal-onset spinal muscular atrophy with congenital bone fractures (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
4 |
X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
4 |
NEK9-related lethal skeletal dysplasia |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Joint contractures, developmental delay, Pierre Robin syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
5 |
Spondyloepiphyseal dysplasia Stanescu type |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
4 |
Arthrofibrosis |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Myosin binding protein C1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
4 |
Hypermobility syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Hypermobile Ehlers-Danlos syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
5 |
Generalized benign joint hypermobility |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Localised benign joint hypermobility |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Myopathic Ehlers-Danlos syndrome (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
6 |
Classical-like Ehlers-Danlos syndrome type 2 |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
6 |
Congenital contracture of limbs and face, hypotonia, developmental delay syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Antenatal multi-minicore disease with arthrogryposis multiplex congenita |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Diastrophic dysplasia |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
4 |
Arthrogryposis multiplex congenita |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Pena-Shokeir syndrome type I (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Marden Walker syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Microphthalmia, microtia, fetal akinesia syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
7 |
Hecht syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Congenital muscular dystrophy with arthrogryposis multiplex congenita |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
3 |
Congenital amyoplasia (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |
Ehlers-Danlos and osteogenesis imperfecta syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
7 |
Spondyloepimetaphyseal dysplasia with joint laxity Beighton type |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
4 |
Spondyloepimetaphyseal dysplasia with joint laxity exocyst complex component 6B type (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
5 |
Congenital pontocerebellar hypoplasia type 12 |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
7 |
Alkuraya Kucinskas syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
5 |
Progressive flexion contracture of joint (disorder) |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Some |
2 |