Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Standing height |
Is a |
True |
Body height (observable entity) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Recumbent body height (observable entity) |
Is a |
True |
Body height (observable entity) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pre-amputation measured body height (observable entity) |
Is a |
True |
Body height (observable entity) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Estimated body height |
Is a |
True |
Body height (observable entity) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
The stated length of the body. |
Is a |
True |
Body height (observable entity) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome (disorder) |
Interprets |
True |
Body height (observable entity) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Severe myopia, generalized joint laxity, short stature syndrome |
Interprets |
True |
Body height (observable entity) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
QRICH1-related intellectual disability, chondrodysplasia syndrome |
Interprets |
True |
Body height (observable entity) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
A rare mitochondrial disease characterised by a highly variable phenotypic spectrum comprising delayed motor development, peripheral neuropathy, cataract, short stature due to growth hormone deficiency, nystagmus, sensorineural hearing loss, dysmorphic facial features, and skeletal abnormalities consistent with spondyloepimetaphyseal dysplasia. Hyperextensible joints, achalasia, and telangiectasia have also been described. Cognition is normal. Atrophy of the pituitary gland has been observed in brain imaging. |
Interprets |
True |
Body height (observable entity) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |
Microcephalic primordial dwarfism, insulin resistance syndrome (disorder) |
Interprets |
True |
Body height (observable entity) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome |
Interprets |
True |
Body height (observable entity) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Leri-Weill dyschondrosteosis |
Interprets |
True |
Body height (observable entity) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
8 |