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722107005: Ossification anomaly with psychomotor developmental delay syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3330718016 Ossification anomaly with psychomotor developmental delay syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330719012 Ossification anomaly with psychomotor developmental delay syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5402823015 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402824014 A rare primary bone dysplasia characterised by global developmental delay, hypotonia, ossification anomalies of the cranial vault, abnormalities of the long bones due to defective remodelling, thoracic deformity, and progressive osteopenia. Dysmorphic craniofacial features include microcephaly, hypertelorism, narrow mouth, cleft palate, and micrognathia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3330718016 Ossification anomaly with psychomotor developmental delay syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3330718016 Ossification anomaly with psychomotor developmental delay syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330719012 Ossification anomaly with psychomotor developmental delay syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3330719012 Ossification anomaly with psychomotor developmental delay syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3330720018 This syndrome has characteristics of hypomineralisation of the cranial bones, thoracic dystrophy, hypotonia and abnormal and slender long bones due to an alteration in remodelling during ossification. It has been described in two brothers and was present at birth. The surviving boy displayed progressive osteopenia, slow healing of the periostal anomalies, hepatic angiomas, a thoracic deformity, delayed tooth eruption, progressive microcephaly with dilation of the cerebral ventricles and mental and motor delay. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3330724010 This syndrome has characteristics of hypomineralization of the cranial bones, thoracic dystrophy, hypotonia and abnormal and slender long bones due to an alteration in remodelling during ossification. It has been described in two brothers and was present at birth. The surviving boy displayed progressive osteopenia, slow healing of the periostal anomalies, hepatic angiomas, a thoracic deformity, delayed tooth eruption, progressive microcephaly with dilation of the cerebral ventricles and mental and motor delay. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402823015 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. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402824014 A rare primary bone dysplasia characterised by global developmental delay, hypotonia, ossification anomalies of the cranial vault, abnormalities of the long bones due to defective remodelling, thoracic deformity, and progressive osteopenia. Dysmorphic craniofacial features include microcephaly, hypertelorism, narrow mouth, cleft palate, and micrognathia. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3416591001000113 Ossifikationsstörung - psychomotorische Entwicklungsverzögerung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
882971000172116 syndrome d'anomalies de l'ossification-retard psychomoteur fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
882971000172116 syndrome d'anomalies de l'ossification-retard psychomoteur fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3416591001000113 Ossifikationsstörung - psychomotorische Entwicklungsverzögerung de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ossification anomaly with psychomotor developmental delay syndrome Is a retard mental false Inferred relationship Existential restriction modifier (core metadata concept)
Ossification anomaly with psychomotor developmental delay syndrome Is a Disorder of thorax (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Ossification anomaly with psychomotor developmental delay syndrome Is a Dysplasia with defective mineralization true Inferred relationship Existential restriction modifier (core metadata concept)
Ossification anomaly with psychomotor developmental delay syndrome Is a Degenerative disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Ossification anomaly with psychomotor developmental delay syndrome Associated morphology Dystrophy false Inferred relationship Existential restriction modifier (core metadata concept) 3
Ossification anomaly with psychomotor developmental delay syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Ossification anomaly with psychomotor developmental delay syndrome Finding site Thoracic structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Ossification anomaly with psychomotor developmental delay syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 4
Ossification anomaly with psychomotor developmental delay syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Ossification anomaly with psychomotor developmental delay syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Ossification anomaly with psychomotor developmental delay syndrome Is a Intelligenzminderung true Inferred relationship Existential restriction modifier (core metadata concept)
Ossification anomaly with psychomotor developmental delay syndrome Is a Congenital anomaly of thorax true Inferred relationship Existential restriction modifier (core metadata concept)
Ossification anomaly with psychomotor developmental delay syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Ossification anomaly with psychomotor developmental delay syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Ossification anomaly with psychomotor developmental delay syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Ossification anomaly with psychomotor developmental delay syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Ossification anomaly with psychomotor developmental delay syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Ossification anomaly with psychomotor developmental delay syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier (core metadata concept) 1
Ossification anomaly with psychomotor developmental delay syndrome Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Ossification anomaly with psychomotor developmental delay syndrome Finding site Thoracic structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Ossification anomaly with psychomotor developmental delay syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 2
Ossification anomaly with psychomotor developmental delay syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Ossification anomaly with psychomotor developmental delay syndrome Associated morphology Impaired mineralization (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Ossification anomaly with psychomotor developmental delay syndrome Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Ossification anomaly with psychomotor developmental delay syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Ossification anomaly with psychomotor developmental delay syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Ossification anomaly with psychomotor developmental delay syndrome Interprets Adaptation behavior true Inferred relationship Existential restriction modifier (core metadata concept) 5
Ossification anomaly with psychomotor developmental delay syndrome Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 5

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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