FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

24559001: Mutilating keratoderma (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1223673015 Vohwinkel's mutilating keratoderma en Synonym Active Case sensitive SNOMED CT core
41186015 Mutilating keratoderma en Synonym Active Case insensitive SNOMED CT core
4589802013 Keratoderma hereditarium mutilans en Synonym Active Case insensitive SNOMED CT core
4589803015 Mutilating keratoderma of Vohwinkel en Synonym Active Initial character case insensitive SNOMED CT core
4589804014 Vohwinkel syndrome en Synonym Active Case sensitive SNOMED CT core
754208012 Mutilating keratoderma (disorder) en Fully specified name Active Case insensitive SNOMED CT core


1 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Mutilating keratoderma Associated morphology Hyperkeratosis true Inferred relationship Some 3
Mutilating keratoderma Finding site Skin structure of palmar area of hand true Inferred relationship Some 2
Mutilating keratoderma Finding site Skin structure of sole of foot true Inferred relationship Some 3
Mutilating keratoderma Is a Rough skin of hands true Inferred relationship Some
Mutilating keratoderma Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Mutilating keratoderma Is a Erythrokeratoderma true Inferred relationship Some
Mutilating keratoderma Is a Auditory system hereditary disorder true Inferred relationship Some
Mutilating keratoderma Is a Congenital sensorineural hearing loss true Inferred relationship Some
Mutilating keratoderma Interprets Hearing true Inferred relationship Some 4
Mutilating keratoderma Has interpretation Impaired true Inferred relationship Some 4
Mutilating keratoderma Occurrence Congenital true Inferred relationship Some 5
Mutilating keratoderma Finding site Structure of auditory system true Inferred relationship Some 5
Mutilating keratoderma Has definitional manifestation Abnormal keratinisation false Inferred relationship Some
Mutilating keratoderma Associated morphology Congenital anomaly false Inferred relationship Some 1
Mutilating keratoderma Is a Congenital keratoderma false Inferred relationship Some
Mutilating keratoderma Is a Hereditary palmoplantar keratoderma true Inferred relationship Some
Mutilating keratoderma Finding site Skin structure false Inferred relationship Some 1
Mutilating keratoderma Finding site Skin structure false Inferred relationship Some 1
Mutilating keratoderma Finding site Skin structure false Inferred relationship Some 2
Mutilating keratoderma Finding site Skin structure false Inferred relationship Some 1
Mutilating keratoderma Finding site Skin structure false Inferred relationship Some 2
Mutilating keratoderma Finding site Skin structure false Inferred relationship Some 1
Mutilating keratoderma Finding site Skin structure false Inferred relationship Some 2
Mutilating keratoderma Finding site Skin structure false Inferred relationship Some 1
Mutilating keratoderma Finding site Skin structure false Inferred relationship Some 2
Mutilating keratoderma Finding site Skin structure false Inferred relationship Some 1
Mutilating keratoderma Finding site Skin structure false Inferred relationship Some 2
Mutilating keratoderma Occurrence Congenital false Inferred relationship Some 3
Mutilating keratoderma Finding site Skin structure false Inferred relationship Some 3
Mutilating keratoderma Associated morphology Developmental abnormality false Inferred relationship Some 3
Mutilating keratoderma Occurrence Congenital false Inferred relationship Some 4
Mutilating keratoderma Associated morphology Hyperkeratosis false Inferred relationship Some 4
Mutilating keratoderma Finding site Skin structure false Inferred relationship Some 4
Mutilating keratoderma Occurrence Congenital false Inferred relationship Some
Mutilating keratoderma Associated morphology Hyperkeratosis true Inferred relationship Some 2
Mutilating keratoderma Finding site Skin structure false Inferred relationship Some 2
Mutilating keratoderma Has interpretation Abnormal true Inferred relationship Some 1
Mutilating keratoderma Interprets Keratinisation true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Keratoderma hereditarium mutilans with ichthyosis syndrome Is a True Mutilating keratoderma Inferred relationship Some
Autosomal dominant mutilating keratoderma Is a False Mutilating keratoderma Inferred relationship Some
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Is a False Mutilating keratoderma Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start