FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

778022009: Ehlers-Danlos syndrome due to tenascin-X deficiency (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3737231017 Ehlers-Danlos syndrome due to tenascin-X deficiency en Synonym Active Entire term case sensitive SNOMED CT core module
3737232012 Ehlers-Danlos syndrome due to tenascin-X deficiency (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3737233019 Ehlers-Danlos syndrome classic-like type 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
Ehlers-Danlos syndrome due to tenascin-X deficiency Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Ehlers-Danlos syndrome due to tenascin-X deficiency Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Ehlers-Danlos syndrome due to tenascin-X deficiency Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
Ehlers-Danlos syndrome due to tenascin-X deficiency Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Ehlers-Danlos syndrome due to tenascin-X deficiency Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 2
Ehlers-Danlos syndrome due to tenascin-X deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Ehlers-Danlos syndrome due to tenascin-X deficiency Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Ehlers-Danlos syndrome due to tenascin-X deficiency Finding site Skin structure true Inferred relationship Existential restriction modifier 2
Ehlers-Danlos syndrome due to tenascin-X deficiency Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Ehlers-Danlos syndrome due to tenascin-X deficiency Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Ehlers-Danlos syndrome due to tenascin-X deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Ehlers-Danlos syndrome due to tenascin-X deficiency Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
Ehlers-Danlos syndrome due to tenascin-X deficiency Is a Ehlers-Danlos syndrome true Inferred relationship Existential restriction modifier
Ehlers-Danlos syndrome due to tenascin-X deficiency Finding site Connective tissue structure true Inferred relationship Existential restriction modifier 3
Ehlers-Danlos syndrome due to tenascin-X deficiency Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Ehlers-Danlos syndrome due to tenascin-X deficiency Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Ehlers-Danlos syndrome due to tenascin-X deficiency Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start