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

724002003: Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification 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
3428520010 Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3428521014 Rambaud Gallian syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3428522019 Rambaud Gallian Touchard syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3428523012 Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3428524018 Retinal ischaemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification 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
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome Is a Cerebral calcification true Inferred relationship Existential restriction modifier
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome Is a Retinal ischemia true Inferred relationship Existential restriction modifier
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome Is a Vascular degeneration true Inferred relationship Existential restriction modifier
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome Is a Cardiovascular system hereditary disorder true Inferred relationship Existential restriction modifier
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome Is a Hereditary disorder of nervous system false Inferred relationship Existential restriction modifier
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome Finding site Retinal structure true Inferred relationship Existential restriction modifier 2
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome Associated morphology Hyaline degeneration true Inferred relationship Existential restriction modifier 4
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome Finding site Structure of small blood vessel (organ) true Inferred relationship Existential restriction modifier 4
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome Associated morphology Pathologic calcification, calcified structure true Inferred relationship Existential restriction modifier 5
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome Finding site Structure of cerebrum true Inferred relationship Existential restriction modifier 5
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome Is a Hereditary degenerative disease of central nervous system true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start