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

367601000119103: Hereditary amyloidosis (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3482130011 Hereditary amyloidosis (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3482131010 Hereditary amyloidosis en Synonym Active Entire term case insensitive SNOMED CT core module

29 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary amyloidosis Associated morphology Amyloid deposition true Inferred relationship Existential restriction modifier 1
Hereditary amyloidosis Is a Amyloidosis true Inferred relationship Existential restriction modifier
Hereditary amyloidosis Is a Hereditary disease true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Familial Mediterranean fever Is a False Hereditary amyloidosis Inferred relationship Existential restriction modifier
Familial amyloid nephropathy with urticaria AND deafness Is a True Hereditary amyloidosis Inferred relationship Existential restriction modifier
Hereditary oculoleptomeningeal amyloid angiopathy Is a True Hereditary amyloidosis Inferred relationship Existential restriction modifier
Familial amyloid polyneuropathy with cutaneous amyloidosis Is a False Hereditary amyloidosis Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Type II Is a False Hereditary amyloidosis Inferred relationship Existential restriction modifier
Transthyretin related familial amyloid cardiomyopathy Is a True Hereditary amyloidosis Inferred relationship Existential restriction modifier
Autosomal dominant beta2-microglobulinic amyloidosis Is a True Hereditary amyloidosis Inferred relationship Existential restriction modifier
Hereditary cerebral hemorrhage with amyloidosis Is a False Hereditary amyloidosis Inferred relationship Existential restriction modifier
Prion protein systemic amyloidosis Is a True Hereditary amyloidosis Inferred relationship Existential restriction modifier
Familial dementia British type Is a False Hereditary amyloidosis Inferred relationship Existential restriction modifier
Hereditary gelsolin amyloidosis Is a True Hereditary amyloidosis Inferred relationship Existential restriction modifier
Familial dementia Danish type Is a False Hereditary amyloidosis Inferred relationship Existential restriction modifier
Meretoja syndrome Is a False Hereditary amyloidosis Inferred relationship Existential restriction modifier
Heredofamilial systemic amyloidosis affecting skin Is a True Hereditary amyloidosis Inferred relationship Existential restriction modifier
Familial amyloid polyneuropathy Is a True Hereditary amyloidosis Inferred relationship Existential restriction modifier
Gelatinous droplike corneal dystrophy Is a True Hereditary amyloidosis Inferred relationship Existential restriction modifier
Hereditary cystatin C amyloid angiopathy Is a False Hereditary amyloidosis Inferred relationship Existential restriction modifier
Lattice corneal dystrophy Is a False Hereditary amyloidosis Inferred relationship Existential restriction modifier
Localized hereditary amyloidosis Is a True Hereditary amyloidosis Inferred relationship Existential restriction modifier
Hereditary cerebrovascular amyloidosis Is a True Hereditary amyloidosis Inferred relationship Existential restriction modifier
Integral membrane protein 2B related amyloidosis Is a True Hereditary amyloidosis Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start