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721229003: Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
3324684019 Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3324685018 Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
3324686017 Ferlini Ragno Calzolari syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3324687014 Waaler Aarskog syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Is a Congenital hydrocephalus true Inferred relationship Existential restriction modifier
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Is a Congenital elevation of scapula true Inferred relationship Existential restriction modifier
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Is a Hereditary disorder of nervous system true Inferred relationship Existential restriction modifier
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier 3
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Finding site Structure of brain cerebrospinal fluid pathway false Inferred relationship Existential restriction modifier 3
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Finding site Bone structure of scapula false Inferred relationship Existential restriction modifier 4
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Finding site Bone structure of scapula false Inferred relationship Existential restriction modifier 5
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 4
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Associated morphology Superior displacement false Inferred relationship Existential restriction modifier 5
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Associated morphology Superior displacement true Inferred relationship Existential restriction modifier 1
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Finding site Structure of brain cerebrospinal fluid pathway true Inferred relationship Existential restriction modifier 2
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Finding site Bone structure of scapula true Inferred relationship Existential restriction modifier 1
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Associated morphology Congenital dilatation false Inferred relationship Existential restriction modifier 2
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Associated morphology Dilatation true Inferred relationship Existential restriction modifier 2
Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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