Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Hypocalcification |
Is a |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Dental caries associated with enamel hypomineralization (disorder) |
Associated morphology |
False |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Enamel hypomineralization (disorder) |
Associated morphology |
False |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Localized enamel hypomineralization of undetermined etiology (disorder) |
Associated morphology |
False |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Localized enamel hypomineralization associated with localized trauma |
Associated morphology |
False |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Localized enamel hypomineralization associated with localized infection (disorder) |
Associated morphology |
False |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Generalised enamel hypomineralisation |
Associated morphology |
False |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hypocalcification of teeth (disorder) |
Associated morphology |
False |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hypocalcification of teeth (disorder) |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Localized enamel hypomineralization of undetermined etiology (disorder) |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Enamel hypomineralization (disorder) |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Generalised enamel hypomineralisation |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Localized enamel hypomineralization associated with localized infection (disorder) |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Localized enamel hypomineralization associated with localized trauma |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Molar incisor hypomineralisation |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Amelogenesis imperfecta, hypocalcification type |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hypophosphatemic rickets with nephrotic-glycosuric dwarfism |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Autosomal dominant hypophosphatemic rickets |
Associated morphology |
False |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Autosomal dominant hypophosphatemic bone disease |
Associated morphology |
False |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Dysplasia with defective mineralization |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Ossification anomaly with psychomotor developmental delay syndrome |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis |
Associated morphology |
False |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
4 |
Familial x-linked hypophosphatemic vitamin D refractory rickets |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Autosomal dominant hypophosphatemic rickets |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Autosomal dominant hypophosphatemic bone disease |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
A rare ciliopathy characterized by congenital cataract with secondary glaucoma, developmental delay, short stature, multiple skeletal abnormalities (spinal deformities, limb anomalies, delayed bone age), dental anomalies (oligodontia, enamel defects), dysmorphic facial features (including coarse facies, low hairline, epicanthal folds, flat and broad nasal bridges, and retrognathia), and stroke. Other recurrent manifestations are hearing loss and nephrocalcinosis. |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hypomineralisation of enamel of second primary molar tooth |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hypomineralization of enamel of teeth (disorder) |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hypomineralization of tooth (disorder) |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Hypomineralisation of enamel of molar tooth |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Molar incisor hypomineralisation |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Rickets due to prematurity (disorder) |
Associated morphology |
True |
Impaired mineralization (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |