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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
1812321000195114 milio it 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 false Inferred relationship Some
Milium Is a Keratinizing cyst (morphologic abnormality) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Expression of comedones and milia Indirect morphology (attribute) False Milium Inferred relationship Some 1
Multiple eruptive milia Associated morphology False Milium Inferred relationship Some 1
Milia Associated morphology False Milium Inferred relationship Some 1
Primary milia Associated morphology False Milium Inferred relationship Some 1
Secondary milia Associated morphology False Milium Inferred relationship Some 1
kyste milial Associated morphology False Milium Inferred relationship Some 1
Multiple milia Associated morphology False Milium Inferred relationship Some 1
Neonatal milia (disorder) Associated morphology False Milium Inferred relationship Some 1
Milia of eyelid Associated morphology False Milium Inferred relationship Some 1
On examination milia Associated morphology False Milium Inferred relationship Some 1
Neonatal milia (disorder) Associated morphology True Milium Inferred relationship Some 1
Multiple milia Associated morphology False Milium Inferred relationship Some 1
On examination milia Associated morphology False Milium Inferred relationship Some 1
Multiple eruptive milia Associated morphology True Milium Inferred relationship Some 1
Secondary milia Associated morphology True Milium Inferred relationship Some 1
kyste milial Associated morphology False Milium Inferred relationship Some 1
Primary milia Associated morphology True Milium Inferred relationship Some 1
Milia Associated morphology True Milium Inferred relationship Some 1
Milia of eyelid Associated morphology True Milium Inferred relationship Some 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 Some 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 Some 1

This concept is not in any reference sets

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