| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Lethal congenital contracture syndrome type 2 |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Lethal congenital contracture syndrome type 3 |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Foot joint - range of movement |
Is a |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
|
| Hand joint range of movement |
Is a |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
|
| Inherited arthrogryposis |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Malignant hyperthermia with arthrogryposis and torticollis syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
4 |
| X-linked lethal multiple pterygium syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Fetal akinesia, cerebral and retinal hemorrhage syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Contracture with ectodermal dysplasia and orofacial cleft syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
7 |
| Neurogenic arthrogryposis multiplex congenita |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Autosomal dominant multiple pterygium syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Distal arthrogryposis type 5D |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Joint contracture, webbed neck, micrognathia, hypoplastic nipple syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
5 |
| Larsen-like syndrome beta-1,3-glucuronyltransferase 3 type |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
4 |
| Congenital neuropathy with arthrogryposis multiplex congenita |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Arthrogryposis with renal dysfunction and cholestasis syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Camptodactyly with joint contracture and facial skeletal defect syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Camptobrachydactyly |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
4 |
| Autism spectrum disorder, epilepsy, arthrogryposis syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Lethal arthrogryposis co-occurrent with anterior horn cell disease |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Contracture of joint |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Distal arthrogryposis type 1 |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Neurogenic arthrogryposis multiplex congenita |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
4 |
| On examination - reduced joint movement |
Interprets |
False |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
4 |
| On examination - reduced movement of spine |
Interprets |
False |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| On examination - reduced movement of arm |
Interprets |
False |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Holoprosencephaly sequence with hypokinesia and congenital joint contracture syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
4 |
| Contracture of multiple joints |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| German syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
1 |
| Contracture of joint following injury |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Lethal congenital contracture syndrome type 1 |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Congenital arthrogryposis caused by teratogen |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| On examination - reduced movement of wrist |
Interprets |
False |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Hydrocephalus with cleft palate and joint contracture syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
9 |
| Distal arthrogryposis syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Temporomandibular joint stiff |
Interprets |
False |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
1 |
| Arthrogryposis and ectodermal dysplasia syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
6 |
| Arthrogryposis with renal dysfunction and cholestasis syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
4 |
| Arthrogryposis-like syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Congenital contractural arachnodactyly |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Multiple stiff joints |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
1 |
| Morning stiffness - joint |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
1 |
| Marfanoid joint hypermobility syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Hypermobility of joint |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
1 |
| Spondyloepimetaphyseal dysplasia with joint laxity |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
4 |
| Distal arthrogryposis type 3 |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Prenatal-onset spinal muscular atrophy with congenital bone fractures |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
4 |
| X-linked keloid scarring, reduced joint mobility, increased optic cup-to-disc ratio syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
4 |
| NIMA related kinase 9 lethal skeletal dysplasia |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Joint contractures, developmental delay, Pierre Robin syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
5 |
| Spondyloepiphyseal dysplasia Stanescu type |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
4 |
| Arthrofibrosis |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
2 |
| Myosin binding protein C1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
4 |
| Hypermobility syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Hypermobile Ehlers-Danlos syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
5 |
| Generalized benign joint hypermobility |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Localized benign joint hypermobility |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Myopathic Ehlers-Danlos syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
6 |
| Classical-like Ehlers-Danlos syndrome type 2 |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
6 |
| Congenital contracture of limbs and face, hypotonia, developmental delay syndrome |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Antenatal multi-minicore disease with arthrogryposis multiplex congenita |
Interprets |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
3 |
| Beighton 9-point scoring system for joint hypermobility score |
Is a |
True |
Range of joint movement |
Inferred relationship |
Existential restriction modifier |
|