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24559001: Mutilating keratoderma (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

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


1 descendants. Search Descendants:

Expanded Value Set


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

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

This concept is not in any reference sets

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