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63246000: Cholestanol storage disease (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
105135015 Cholestanol storage disease en Synonym Active Entire term case insensitive SNOMED CT core module
105136019 Cerebrotendinous xanthomatosis en Synonym Active Entire term case insensitive SNOMED CT core module
105137011 Cerebral cholesterinosis en Synonym Active Entire term case insensitive SNOMED CT core module
105138018 van Bogaert-Scherer-Epstein syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
499521015 CTX - Cerebrotendinous xanthomatosis en Synonym Active Entire term case sensitive SNOMED CT core module
499522010 Cerebrotendinous cholesterinosis en Synonym Active Entire term case insensitive SNOMED CT core module
499523017 Cholestanolosis en Synonym Active Entire term case insensitive SNOMED CT core module
499524011 Van Bogaert-Scherer-Epstein disease en Synonym Active Only initial character case insensitive SNOMED CT core module
802508019 Cholestanol storage disease (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cholestanol storage disease Is a Xanthomatosis true Inferred relationship Existential restriction modifier
Cholestanol storage disease Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Cholestanol storage disease Is a Familial disease with storage of sterols (other than cholesterol) false Inferred relationship Existential restriction modifier
Cholestanol storage disease Is a Disorder of cholesterol catabolism true Inferred relationship Existential restriction modifier
Cholestanol storage disease Occurrence Congenital false Inferred relationship Existential restriction modifier
Cholestanol storage disease Finding site Skin structure true Inferred relationship Existential restriction modifier 2
Cholestanol storage disease Is a Congenital anomaly of integument false Inferred relationship Existential restriction modifier
Cholestanol storage disease Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Cholestanol storage disease Is a Synthetic defect of bile acids true Inferred relationship Existential restriction modifier
Cholestanol storage disease Is a Digestive system hereditary disorder false Inferred relationship Existential restriction modifier
Cholestanol storage disease Finding site Liver structure false Inferred relationship Existential restriction modifier 1
Cholestanol storage disease Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Cholestanol storage disease Finding site Liver structure true Inferred relationship Existential restriction modifier 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Ataxia co-occurrent and due to cerebrotendinous xanthomatosis Due to False Cholestanol storage disease Inferred relationship Existential restriction modifier 3
Ataxia co-occurrent and due to cerebrotendinous xanthomatosis Is a False Cholestanol storage disease Inferred relationship Existential restriction modifier
Ataxia due to cerebrotendinous xanthomatosis Due to True Cholestanol storage disease Inferred relationship Existential restriction modifier 1

This concept is not in any reference sets

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