| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Branchial dysplasia, intellectual disability, inguinal hernia syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| High bone mass osteogenesis imperfecta |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Leukoencephalopathy with metaphyseal chondrodysplasia syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Larsen-like osseous dysplasia, short stature syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Spondylometaphyseal dysplasia A4 type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Congenital dysplasia of cardiac valve |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Acrocapitofemoral dysplasia |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Robinson nail dystrophy-deafness syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
3 |
| Ulna fibula ray defect and brachydactyly syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
4 |
| Ulna fibula ray defect and brachydactyly syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
3 |
| Autosomal recessive hypohidrotic ectodermal dysplasia syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Acropectorovertebral dysplasia |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Microcephalic osteodysplastic dysplasia Saul Wilson type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Hypertelorism Teebi type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Spondyloepimetaphyseal dysplasia Irapa type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Omodysplasia |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Bone dysplasia lethal Holmgren type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Ectodermal dysplasia and sensorineural deafness syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Dysspondyloenchondromatosis |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Mesomelic dysplasia Kantaputra type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Frontonasal dysplasia with alopecia and genital anomaly syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Hereditary mucoepithelial dysplasia |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Dysplasia epiphysealis hemimelica |
Associated morphology |
False |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Hip dysplasia with enchondromata and ecchondroma syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Mesomelic dysplasia Savarirayan type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Spondyloenchondromatosis |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Spondyloepimetaphyseal dysplasia 3-prime-phosphoadenosine 5-prime-phosphosulfate synthase 2 type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Brachydactyly and arterial hypertension syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Osteogenesis imperfecta type I |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| 12q14 microdeletion syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
3 |
| Mild spondyloepiphyseal dysplasia with premature onset arthrosis |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Robinow syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
4 |
| Mesomelic dysplasia of hypoplastic ulna and fibula type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Spondyloepimetaphyseal dysplasia, abnormal dentition syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Short stature Brussels type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Multiple epiphyseal dysplasia type 5 |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Genochondromatosis |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Acrofacial dysostosis Palagonia type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Acrofacial dysostosis Palagonia type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Dysplasia of left kidney |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Polyostotic fibrous dysplasia of bone |
Associated morphology |
False |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Epilepsy, microcephaly, skeletal dysplasia syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Coxopodopatellar syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Heart-hand syndrome Slovenian type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Autosomal dominant hypohidrotic ectodermal dysplasia syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Lethal chondrodysplasia with fragmented bone |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Oro-facial digital syndrome type 13 |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
6 |
| Roifman syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Cleidorhizomelic syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Precocious osteodysplasty |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Dysplasia of head of femur Meyer type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Heart-hand syndrome type 2 |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Chondrodysplasia punctata, Conradi-Hünermann type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Spondyloepimetaphyseal dysplasia with multiple dislocations |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Hallermann-Streiff syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Multiple epiphyseal dysplasia Al-Gazali type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| X-linked dominant chondrodysplasia punctata of Happle |
Associated morphology |
False |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Spondyloepiphyseal dysplasia with myopia and sensorineural deafness syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Multiple epiphyseal dysplasia Lowry type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Conductive deafness, ptosis, skeletal anomalies syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Conductive deafness, ptosis, skeletal anomalies syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Ossification anomaly with psychomotor developmental delay syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Rhizomelic dysplasia of Patterson Lowry type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Craniometadiaphyseal dysplasia wormian bone type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Clastothrix |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Metaphyseal chondrodysplasia, McKusick type with associated immunodeficiency |
Associated morphology |
False |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Spondyloepimetaphyseal dysplasia Shohat type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Exostosis, anetoderma, brachydactyly type E syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Acrodysplasia scoliosis |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Severe lateral tibial bowing with short stature |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Limb mammary syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Absent radius, anogenital anomalies syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Stern Lubinsky Durrie syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Acroscyphodysplasia |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Cerebrofacial dysplasia |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Dolichospondylic dysplasia |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Czech dysplasia metatarsal type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Ehlers-Danlos and osteogenesis imperfecta syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Ehlers-Danlos and osteogenesis imperfecta syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Short stature homeobox related short stature |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Deafness with skeletal dysplasia and lip granuloma syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Secondary renal dysplasia |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Larsen-like syndrome beta-1,3-glucuronyltransferase 3 type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Multiple epiphyseal dysplasia type 1 |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Brachydactyly elbow wrist dysplasia |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Brachydactyly elbow wrist dysplasia |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Coloboma of macula with brachydactyly type B syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Camptodactyly and tall stature with scoliosis and hearing loss syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
3 |
| Axial spondylometaphyseal dysplasia |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Ectodermal dysplasia with hair-nail defect |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
3 |
| X-linked calvarial hyperostosis |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Jeune thoracic dystrophy |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Hypomandibular faciocranial dysostosis |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Patterson Stevenson Fontaine syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Patterson Stevenson Fontaine syndrome |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |
| Familial osteodysplasia Anderson type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
2 |
| Familial osteodysplasia Anderson type |
Associated morphology |
True |
Dysplasia |
Inferred relationship |
Existential restriction modifier |
1 |