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128416000: Impaired mineralization (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
206716015 Impaired mineralization en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
474392010 Impaired mineralisation en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
732406017 Impaired mineralization (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Impaired mineralization Is a Maturation defect true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Hypocalcification Is a True Impaired mineralization Inferred relationship Some
Dental caries associated with enamel hypomineralization Associated morphology False Impaired mineralization Inferred relationship Some 2
Enamel hypomineralization (disorder) Associated morphology False Impaired mineralization Inferred relationship Some 1
Localized enamel hypomineralization of undetermined etiology Associated morphology False Impaired mineralization Inferred relationship Some 1
Localized enamel hypomineralization associated with localized trauma Associated morphology False Impaired mineralization Inferred relationship Some 1
Localized enamel hypomineralization associated with localized infection Associated morphology False Impaired mineralization Inferred relationship Some 1
Generalised enamel hypomineralisation Associated morphology False Impaired mineralization Inferred relationship Some 1
Hypocalcification of teeth Associated morphology False Impaired mineralization Inferred relationship Some 1
Hypocalcification of teeth Associated morphology True Impaired mineralization Inferred relationship Some 1
Localized enamel hypomineralization of undetermined etiology Associated morphology True Impaired mineralization Inferred relationship Some 1
Enamel hypomineralization (disorder) Associated morphology True Impaired mineralization Inferred relationship Some 1
Generalised enamel hypomineralisation Associated morphology True Impaired mineralization Inferred relationship Some 1
Localized enamel hypomineralization associated with localized infection Associated morphology True Impaired mineralization Inferred relationship Some 1
Localized enamel hypomineralization associated with localized trauma Associated morphology True Impaired mineralization Inferred relationship Some 1
Molar incisor hypomineralization Associated morphology True Impaired mineralization Inferred relationship Some 1
Amelogenesis imperfecta, hypocalcification type Associated morphology True Impaired mineralization Inferred relationship Some 1
Hypophosphataemic rickets with nephrotic-glycosuric dwarfism Associated morphology True Impaired mineralization Inferred relationship Some 3
Autosomal dominant hypophosphatemic rickets Associated morphology False Impaired mineralization Inferred relationship Some 3
Autosomal dominant hypophosphataemic bone disease Associated morphology False Impaired mineralization Inferred relationship Some 3
Dysplasia with defective mineralization Associated morphology True Impaired mineralization Inferred relationship Some 2
A rare primary bone dysplasia characterized by global developmental delay, hypotonia, ossification anomalies of the cranial vault, abnormalities of the long bones due to defective remodeling, thoracic deformity, and progressive osteopenia. Dysmorphic craniofacial features include microcephaly, hypertelorism, narrow mouth, cleft palate, and micrognathia. Associated morphology True Impaired mineralization Inferred relationship Some 3
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Associated morphology False Impaired mineralization Inferred relationship Some 4
Familial x-linked hypophosphatemic vitamin D refractory rickets Associated morphology True Impaired mineralization Inferred relationship Some 3
Autosomal dominant hypophosphatemic rickets Associated morphology True Impaired mineralization Inferred relationship Some 2
Autosomal dominant hypophosphataemic bone disease Associated morphology True Impaired mineralization Inferred relationship Some 2
A rare, genetic renal tubular disease characterized by phosphate loss in the proximal tubule, leading to hypercalciuria and recurrent urolithiasis and/or osteoporosis. Associated morphology True Impaired mineralization Inferred relationship Some 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 Inferred relationship Some 2
Hypomineralisation of enamel of second primary molar tooth Associated morphology True Impaired mineralization Inferred relationship Some 1
Hypomineralization of enamel of teeth Associated morphology True Impaired mineralization Inferred relationship Some 1
Hypomineralisation of tooth Associated morphology True Impaired mineralization Inferred relationship Some 1
Hypomineralization of enamel of molar tooth (disorder) Associated morphology True Impaired mineralization Inferred relationship Some 1
Molar incisor hypomineralization Associated morphology True Impaired mineralization Inferred relationship Some 2
Rickets due to prematurity Associated morphology True Impaired mineralization Inferred relationship Some 2

This concept is not in any reference sets

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