FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.2  |  FHIR Version n/a  User: [n/a]

763767006: Erythema palmare hereditarium (disorder)


Status: current, Primitive. Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3643759018 Erythema palmare hereditarium en Synonym Active Case insensitive SNOMED CT core
3643760011 Erythema palmare hereditarium (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3643761010 Red palms disease en Synonym Active Case insensitive SNOMED CT core
3643762015 Lane disease en Synonym Active Case sensitive SNOMED CT core
3643763013 A rare benign congenital genetic skin disorder with characteristics of permanent and asymptomatic erythema of the palmar and less frequently the solar surfaces. In most cases, it presents with sharply demarcated redness of the thenar and hypothenar eminences, as well as the palmar aspect of the phalanges, with scattered telangiectasia spots that do not cause any discomfort (pain, itching or burning) to the patient. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Erythema palmare hereditarium Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Erythema palmare hereditarium Is a Palmar erythema true Inferred relationship Some
Erythema palmare hereditarium Is a Congenital disease true Inferred relationship Some
Erythema palmare hereditarium Is a Hereditary disorder of the integument true Inferred relationship Some
Erythema palmare hereditarium Associated morphology Erythema true Inferred relationship Some 1
Erythema palmare hereditarium Occurrence Congenital true Inferred relationship Some 1
Erythema palmare hereditarium Finding site Skin structure of palmar area of hand true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start