FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.4-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

109470000: Intrinsic enamel discoloration of erythroblastosis fetalis (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
174044015 Intrinsic enamel discoloration of erythroblastosis fetalis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
202820013 Intrinsic enamel discolouration of erythroblastosis foetalis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
338306015 Intrinsic enamel discolouration of erythroblastosis fetalis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
338307012 Intrinsic enamel discoloration of erythroblastosis foetalis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
612313011 Intrinsic enamel discoloration of erythroblastosis fetalis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
174044015 Intrinsic enamel discoloration of erythroblastosis fetalis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
174044015 Intrinsic enamel discoloration of erythroblastosis fetalis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
202820013 Intrinsic enamel discolouration of erythroblastosis foetalis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
202820013 Intrinsic enamel discolouration of erythroblastosis foetalis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
338306015 Intrinsic enamel discolouration of erythroblastosis fetalis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
338306015 Intrinsic enamel discolouration of erythroblastosis fetalis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
338307012 Intrinsic enamel discoloration of erythroblastosis foetalis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
338307012 Intrinsic enamel discoloration of erythroblastosis foetalis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
612313011 Intrinsic enamel discoloration of erythroblastosis fetalis (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
612313011 Intrinsic enamel discoloration of erythroblastosis fetalis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
6350501000241119 décoloration intrinsèque de l'émail dans le cadre d'une maladie hémolytique du fœtus ou du nouveau-né fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6350511000241117 décoloration intrinsèque de l'émail dans le cadre d'une érythroblastose fœtale ou néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6350501000241119 décoloration intrinsèque de l'émail dans le cadre d'une maladie hémolytique du fœtus ou du nouveau-né fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6350511000241117 décoloration intrinsèque de l'émail dans le cadre d'une érythroblastose fœtale ou néonatale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Intrinsic enamel discoloration of erythroblastosis fetalis Is a Intrinsic staining of tooth (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Intrinsic enamel discoloration of erythroblastosis fetalis Is a Color changes during tooth formation true Inferred relationship Existential restriction modifier (core metadata concept)
Intrinsic enamel discoloration of erythroblastosis fetalis Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Intrinsic enamel discoloration of erythroblastosis fetalis Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Intrinsic enamel discoloration of erythroblastosis fetalis Finding site Jaw region structure false Inferred relationship Existential restriction modifier (core metadata concept)
Intrinsic enamel discoloration of erythroblastosis fetalis Finding site Tongue structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Intrinsic enamel discoloration of erythroblastosis fetalis Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 3
Intrinsic enamel discoloration of erythroblastosis fetalis Finding site Enamel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Intrinsic enamel discoloration of erythroblastosis fetalis Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Intrinsic enamel discoloration of erythroblastosis fetalis Associated morphology Abnormal color false Inferred relationship Existential restriction modifier (core metadata concept) 2
Intrinsic enamel discoloration of erythroblastosis fetalis Associated morphology Abnormal color false Inferred relationship Existential restriction modifier (core metadata concept) 1
Intrinsic enamel discoloration of erythroblastosis fetalis Finding site Tooth structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Intrinsic enamel discoloration of erythroblastosis fetalis Is a Disorder of hard tissues of teeth (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Intrinsic enamel discoloration of erythroblastosis fetalis Finding site Face structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Intrinsic enamel discoloration of erythroblastosis fetalis Finding site Oral cavity structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Intrinsic enamel discoloration of erythroblastosis fetalis Has definitional manifestation Abnormal color false Inferred relationship Existential restriction modifier (core metadata concept)
Intrinsic enamel discoloration of erythroblastosis fetalis Finding site Digestive organ structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Intrinsic enamel discoloration of erythroblastosis fetalis Finding site Upper aerodigestive tract structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Intrinsic enamel discoloration of erythroblastosis fetalis Is a Congenital anomaly of jaw (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Intrinsic enamel discoloration of erythroblastosis fetalis Finding site Enamel structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Intrinsic enamel discoloration of erythroblastosis fetalis Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Intrinsic enamel discoloration of erythroblastosis fetalis Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Intrinsic enamel discoloration of erythroblastosis fetalis Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Intrinsic enamel discoloration of erythroblastosis fetalis Finding site Tooth structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Intrinsic enamel discoloration of erythroblastosis fetalis Has definitional manifestation Tooth discolored (finding) false Inferred relationship Existential restriction modifier (core metadata concept)
Intrinsic enamel discoloration of erythroblastosis fetalis Interprets Tooth color (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Intrinsic enamel discoloration of erythroblastosis fetalis Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Intrinsic enamel discoloration of erythroblastosis fetalis Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Intrinsic enamel discoloration of erythroblastosis fetalis Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Intrinsic enamel discoloration of erythroblastosis fetalis Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Intrinsic enamel discoloration of erythroblastosis fetalis Is a Congenital anomaly of tooth (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Intrinsic enamel discoloration of erythroblastosis fetalis Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

Back to Start