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

37719003: Milium (morphologic abnormality)

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
62918018 Milium en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
62919014 Milia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
62920015 Subepidermal keratin cyst en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
62921016 Milium cyst en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
769618011 Milium (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
62918018 Milium en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
62918018 Milium en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
62919014 Milia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
62919014 Milia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
62920015 Subepidermal keratin cyst en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
62920015 Subepidermal keratin cyst en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
62921016 Milium cyst en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
62921016 Milium cyst en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
769618011 Milium (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
769618011 Milium (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1058701000195111 Hautgriess de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
581891000274111 Hautgrieß de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
1058701000195111 Hautgriess de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Milium Is a Cyst (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept)
Milium Is a Keratinizing cyst true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Expression of comedones and milia Indirect morphology False Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple eruptive milia Associated morphology False Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
Milia Associated morphology False Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
Primary milia Associated morphology False Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
Secondary milia Associated morphology False Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
kyste milial Associated morphology False Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple milia Associated morphology False Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal milia (disorder) Associated morphology False Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
Milia of eyelid Associated morphology False Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
On examination milia Associated morphology False Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
Neonatal milia (disorder) Associated morphology True Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple milia Associated morphology False Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
On examination milia Associated morphology False Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
Multiple eruptive milia Associated morphology True Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
Secondary milia Associated morphology True Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
kyste milial Associated morphology False Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
Primary milia Associated morphology True Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
Milia Associated morphology True Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
Milia of eyelid Associated morphology True Milium Inferred relationship Existential restriction modifier (core metadata concept) 1
A rare syndrome characterized by neonatal blisters and milia (small white papules, especially on the face) and congenital absence of dermatoglyphics on the hands and feet. It has been reported in two kindreds (one of which contained 13 affected individuals spanning three generations) and in an unrelated individual. Some affected patients also showed bilateral partial flexion contractures of the fingers and toes, and webbing of the toes. The syndrome is inherited as an autosomal dominant trait. Associated morphology False Milium Inferred relationship Existential restriction modifier (core metadata concept) 2
A rare syndrome characterized by neonatal blisters and milia (small white papules, especially on the face) and congenital absence of dermatoglyphics on the hands and feet. It has been reported in two kindreds (one of which contained 13 affected individuals spanning three generations) and in an unrelated individual. Some affected patients also showed bilateral partial flexion contractures of the fingers and toes, and webbing of the toes. The syndrome is inherited as an autosomal dominant trait. Associated morphology True Milium Inferred relationship Existential restriction modifier (core metadata concept) 1

This concept is not in any reference sets

Back to Start