| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Microcephalic osteodysplastic dysplasia Saul Wilson type (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Muscular dystrophy Selcen type (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Native American myopathy |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Talo-patello-scaphoid osteolysis syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Thoracolaryngopelvic dysplasia |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Grant syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Schimke immuno-osseous dysplasia (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Patterson Stevenson Fontaine syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Short stature, Pierre Robin sequence, cleft mandible, hand anomalies, clubfoot syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Pyogenic arthritis, pyoderma gangrenosum, acne syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Posterior fusion of lumbosacral vertebrae and blepharoptosis syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Frontonasal dysplasia with alopecia and genital anomaly syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Infantile malignant osteopetrosis |
est un(e) (attribut) |
False |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Myopathy due to calsequestrin and sarcoplasmic/endoplasmic reticulum calcium ATPase 1 protein overload (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Mitochondrial myopathy with sideroblastic anemia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Microspherophakia with metaphyseal dysplasia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Metaphyseal dysplasia, maxillary hypoplasia, brachydactyly syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Metaphyseal chondromatosis co-occurrent with D-2 hydroxyglutaric aciduria (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| 8q13 microdeletion syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Laryngeal abductor paralysis with intellectual disability syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Keutel syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Infantile osteopetrosis with neuroaxonal dysplasia syndrome (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Hypospadias, hypertelorism, coloboma, deafness syndrome (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Hypertelorism Teebi type (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| scaphocéphalie familiale type McGillivray |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Autosomal dominant osteopetrosis type 2 (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Cryptomicrotia brachydactyly syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Crisponi syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Craniomicromelic syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Craniometadiaphyseal dysplasia wormian bone type (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Craniolenticulosutural dysplasia (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| raccourcissement congénital du ligament costo-coracoïde |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| X-linked spasticity, intellectual disability, epilepsy syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Omodysplasia (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Microcephalic osteodysplastic primordial dwarfism types I and III (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Familial Scheuermann disease (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Genochondromatosis type 2 (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Short rib polydactyly syndrome type I (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Spastic paraplegia with Paget disease of bone syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Familial chondromalacia of patella (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Intellectual disability, cataract, calcified pinna, myopathy syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Splenogonadal fusion, limb defect, micrognathia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Short stature locking fingers syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Coxoauricular syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Bone dysplasia lethal Holmgren type (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Craniosynostosis fibular aplasia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Cyprus facial neuromusculoskeletal syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Hydrocephalus, tall stature, joint laxity syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Osteopenia, intellectual disability, sparse hair syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Symphalangism with multiple anomalies of hands and feet syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Brachydactyly and distal symphalangism syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Brachydactyly and preaxial hallux varus syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Congenital hypoplasia of ulna and split foot syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Epilepsy, microcephaly, skeletal dysplasia syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Camptobrachydactyly (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Trigonocephaly, short stature, developmental delay syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Absent tibia, polydactyly, arachnoid cyst syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| syndrome de Banki |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Triphalangeal thumb and dislocation of patella syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Camptodactyly taurinuria syndrome (disorder) |
est un(e) (attribut) |
False |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Skeletal dysplasia with wormian bone, multiple fractures, dentinogenesis imperfecta syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| dystrophie thoracique asphyxiante |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Exostosis, anetoderma, brachydactyly type E syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Metaphyseal dysostosis, intellectual disability, conductive deafness syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Long thumb brachydactyly syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Acrocephalopolysyndactyly type II (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Skeletal dysplasia brachydactyly syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Van den Bosch syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Thumb stiffness, brachydactyly, intellectual disability syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Aphalangy, hemivertebra, urogenital, intestinal dysgenesis syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Acrocephalopolysyndactyly type IV (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Summitt syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| 46,XX disorder of sex development with skeletal anomalies syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| SCARF syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Vitamin D-dependent rickets |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Goldenhar syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Geroderma osteodysplastica |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Congenital myopathy with myasthenic-like onset (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Connective tissue disorder due to lysyl hydroxylase-3 deficiency |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| syndrome d'akinésie foetale-hémorragies cérébrales et rétiniennes |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| dyskinésie familiale avec myokymie faciale |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Cerebrofacioarticular syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Velofacioskeletal syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| syndrome de mèches blanches et anomalies multiples |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Deafness, encephaloneuropathy, obesity, valvulopathy syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Dislocation of hip and facial dysmorphism syndrome |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| syndrome de Larsen-like de type B3GAT3 (beta-1,3 glucuronyltransferase 3) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Keipert syndrome (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Spondyloperipheral dysplasia (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Spondyloepimetaphyseal dysplasia Handigodu type |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Myosclerosis (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
| Brachydactyly elbow wrist dysplasia (disorder) |
est un(e) (attribut) |
True |
Hereditary disorder of musculoskeletal system |
Inferred relationship |
Some |
|
FHIR