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70041004: Erythrokeratodermia variabilis (disorder)


Status: current, Primitive. Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
116327014 Erythrokeratodermia variabilis en Synonym Active Case insensitive SNOMED CT core
1233217010 Congenital poikiloderma en Synonym Active Case insensitive SNOMED CT core
1233218017 Mendes da Costa syndrome en Synonym Active Initial character case insensitive SNOMED CT core
810054016 Erythrokeratodermia variabilis (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Erythrokeratodermia variabilis Is a Ichthyosis false Inferred relationship Some
Erythrokeratodermia variabilis Finding site Entire skin true Inferred relationship Some 1
Erythrokeratodermia variabilis Is a Congenital keratoderma true Inferred relationship Some
Erythrokeratodermia variabilis Pathological process Pathological developmental process true Inferred relationship Some 1
Erythrokeratodermia variabilis Is a Congenital anomaly of skin false Inferred relationship Some
Erythrokeratodermia variabilis Occurrence Congenital true Inferred relationship Some 1
Erythrokeratodermia variabilis Is a Developmental hereditary disorder false Inferred relationship Some
Erythrokeratodermia variabilis Is a Autosomal hereditary disorder true Inferred relationship Some
Erythrokeratodermia variabilis Is a Congenital ichthyosis of skin true Inferred relationship Some
Erythrokeratodermia variabilis Associated morphology Congenital anomaly false Inferred relationship Some 2
Erythrokeratodermia variabilis Has definitional manifestation Abnormal keratinisation false Inferred relationship Some
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 2
Erythrokeratodermia variabilis Is a Skin lesion false Inferred relationship Some
Erythrokeratodermia variabilis Is a Erythrokeratoderma false Inferred relationship Some
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 1
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 2
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 1
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 2
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 1
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 2
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 1
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 2
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 1
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 2
Erythrokeratodermia variabilis Occurrence Congenital false Inferred relationship Some 3
Erythrokeratodermia variabilis Associated morphology Developmental abnormality false Inferred relationship Some 3
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 3
Erythrokeratodermia variabilis Finding site Skin structure false Inferred relationship Some 1
Erythrokeratodermia variabilis Occurrence Congenital false Inferred relationship Some
Erythrokeratodermia variabilis Associated morphology Hyperkeratosis true Inferred relationship Some 1
Erythrokeratodermia variabilis Is a Disorder of skin false Inferred relationship Some
Erythrokeratodermia variabilis Has interpretation Abnormal true Inferred relationship Some 2
Erythrokeratodermia variabilis Interprets Keratinisation true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group
MEDNIK syndrome Is a False Erythrokeratodermia variabilis Inferred relationship Some
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Is a False Erythrokeratodermia variabilis Inferred relationship Some
Keratoderma hereditarium mutilans with ichthyosis syndrome Is a False Erythrokeratodermia variabilis Inferred relationship Some
Malignant atrophic papulosis Is a False Erythrokeratodermia variabilis Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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