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723578001: Terminal osseous dysplasia and pigmentary defect syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
3425158015 Terminal osseous dysplasia and pigmentary defect syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3425159011 Terminal osseous dysplasia and pigmentary defect syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Terminal osseous dysplasia and pigmentary defect syndrome Is a Congenital skeletal dysplasia false Inferred relationship Existential restriction modifier
Terminal osseous dysplasia and pigmentary defect syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
Terminal osseous dysplasia and pigmentary defect syndrome Is a Congenital pigmentary skin anomalies false Inferred relationship Existential restriction modifier
Terminal osseous dysplasia and pigmentary defect syndrome Is a Inherited cutaneous hyperpigmentation true Inferred relationship Existential restriction modifier
Terminal osseous dysplasia and pigmentary defect syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Terminal osseous dysplasia and pigmentary defect syndrome Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
Terminal osseous dysplasia and pigmentary defect syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Terminal osseous dysplasia and pigmentary defect syndrome Associated morphology Hyperpigmentation false Inferred relationship Existential restriction modifier 4
Terminal osseous dysplasia and pigmentary defect syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Terminal osseous dysplasia and pigmentary defect syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 4
Terminal osseous dysplasia and pigmentary defect syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 5
Terminal osseous dysplasia and pigmentary defect syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Terminal osseous dysplasia and pigmentary defect syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Terminal osseous dysplasia and pigmentary defect syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 5
Terminal osseous dysplasia and pigmentary defect syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 5
Terminal osseous dysplasia and pigmentary defect syndrome Is a Genetic disorder of skin pigmentation false Inferred relationship Existential restriction modifier
Terminal osseous dysplasia and pigmentary defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Terminal osseous dysplasia and pigmentary defect syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Terminal osseous dysplasia and pigmentary defect syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Terminal osseous dysplasia and pigmentary defect syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Terminal osseous dysplasia and pigmentary defect syndrome Associated morphology Hyperpigmentation true Inferred relationship Existential restriction modifier 1
Terminal osseous dysplasia and pigmentary defect syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Terminal osseous dysplasia and pigmentary defect syndrome Finding site Bone structure true Inferred relationship Existential restriction modifier 2
Terminal osseous dysplasia and pigmentary defect syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 2
Terminal osseous dysplasia and pigmentary defect syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 2
Terminal osseous dysplasia and pigmentary defect syndrome Is a Otopalatodigital syndrome spectrum 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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