Outbound Relationships |
Type |
Target |
Active |
Characteristic |
Refinability |
Group |
Values |
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Is a |
Sensorineural hearing loss |
true |
Inferred relationship |
Existential restriction modifier |
|
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Is a |
Congenital hearing disorder |
false |
Inferred relationship |
Existential restriction modifier |
|
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Is a |
Autosomal dominant retinitis pigmentosa |
true |
Inferred relationship |
Existential restriction modifier |
|
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Is a |
Short stature disorder |
true |
Inferred relationship |
Existential restriction modifier |
|
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Is a |
Osteochondrodysplasia |
false |
Inferred relationship |
Existential restriction modifier |
|
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Is a |
Auditory system hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier |
|
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Is a |
Connective tissue hereditary disorder |
false |
Inferred relationship |
Existential restriction modifier |
|
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Is a |
Hereditary disorder of musculoskeletal system |
true |
Inferred relationship |
Existential restriction modifier |
|
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Finding site |
Structure of auditory system |
true |
Inferred relationship |
Existential restriction modifier |
3 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Interprets |
Hearing, function |
true |
Inferred relationship |
Existential restriction modifier |
4 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Interprets |
Functional observable |
false |
Inferred relationship |
Existential restriction modifier |
|
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Associated morphology |
Dystrophy |
false |
Inferred relationship |
Existential restriction modifier |
7 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Occurrence |
Congenital |
false |
Inferred relationship |
Existential restriction modifier |
7 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Finding site |
Retinal structure |
false |
Inferred relationship |
Existential restriction modifier |
7 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Associated morphology |
Congenital dysplasia |
false |
Inferred relationship |
Existential restriction modifier |
8 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Occurrence |
Congenital |
false |
Inferred relationship |
Existential restriction modifier |
8 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Finding site |
Bone structure |
false |
Inferred relationship |
Existential restriction modifier |
8 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Is a |
Congenital anomaly of retina |
true |
Inferred relationship |
Existential restriction modifier |
|
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Pathological process |
Pathological developmental process |
true |
Inferred relationship |
Existential restriction modifier |
2 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier |
1 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Occurrence |
Congenital |
true |
Inferred relationship |
Existential restriction modifier |
2 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Pathological process |
Pathological developmental process |
true |
Inferred relationship |
Existential restriction modifier |
1 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Associated morphology |
Congenital dysplasia |
false |
Inferred relationship |
Existential restriction modifier |
1 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Finding site |
Retinal structure |
true |
Inferred relationship |
Existential restriction modifier |
2 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Associated morphology |
Dystrophy |
true |
Inferred relationship |
Existential restriction modifier |
2 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Finding site |
Bone structure |
true |
Inferred relationship |
Existential restriction modifier |
1 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Associated morphology |
Dysplasia |
true |
Inferred relationship |
Existential restriction modifier |
1 |
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Is a |
Congenital skeletal dysplasia |
true |
Inferred relationship |
Existential restriction modifier |
|
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Is a |
Congenital anomaly of skeletal bone |
true |
Inferred relationship |
Existential restriction modifier |
|
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Is a |
Developmental hereditary disorder |
true |
Inferred relationship |
Existential restriction modifier |
|
|
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome |
Interprets |
Height / growth measure |
true |
Inferred relationship |
Existential restriction modifier |
5 |
|