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717183001: Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3308613015 Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3308614014 Keratoderma hereditarium mutilans with ichthyosis syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3308615010 Camisa disease en Synonym Active Entire term case sensitive SNOMED CT core module
3308616011 Keratoderma ichthyosiform dermatosis elevated beta-glucuronidase syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3308617019 Vohwinkel ichthyosis syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Keratoderma hereditarium mutilans with ichthyosis syndrome Is a Congenital ichthyosis of skin false Inferred relationship Existential restriction modifier
Keratoderma hereditarium mutilans with ichthyosis syndrome Is a Autosomal dominant mutilating keratoderma false Inferred relationship Existential restriction modifier
Keratoderma hereditarium mutilans with ichthyosis syndrome Has definitional manifestation Abnormal keratinization false Inferred relationship Existential restriction modifier
Keratoderma hereditarium mutilans with ichthyosis syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Keratoderma hereditarium mutilans with ichthyosis syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Keratoderma hereditarium mutilans with ichthyosis syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Keratoderma hereditarium mutilans with ichthyosis syndrome Associated morphology Hyperkeratosis false Inferred relationship Existential restriction modifier 4
Keratoderma hereditarium mutilans with ichthyosis syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Keratoderma hereditarium mutilans with ichthyosis syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 4
Keratoderma hereditarium mutilans with ichthyosis syndrome Has interpretation Abnormal true Inferred relationship Existential restriction modifier 2
Keratoderma hereditarium mutilans with ichthyosis syndrome Interprets Keratinization, function true Inferred relationship Existential restriction modifier 2
Keratoderma hereditarium mutilans with ichthyosis syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Keratoderma hereditarium mutilans with ichthyosis syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Keratoderma hereditarium mutilans with ichthyosis syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Keratoderma hereditarium mutilans with ichthyosis syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 1
Keratoderma hereditarium mutilans with ichthyosis syndrome Is a Autosomal dominant ichthyosis true Inferred relationship Existential restriction modifier
Keratoderma hereditarium mutilans with ichthyosis syndrome Is a Erythrokeratodermia variabilis false Inferred relationship Existential restriction modifier
Keratoderma hereditarium mutilans with ichthyosis syndrome Finding site Entire skin true Inferred relationship Existential restriction modifier 1
Keratoderma hereditarium mutilans with ichthyosis syndrome Finding site Skin structure of palmar area of hand false Inferred relationship Existential restriction modifier 3
Keratoderma hereditarium mutilans with ichthyosis syndrome Interprets Keratinization, function false Inferred relationship Existential restriction modifier 3
Keratoderma hereditarium mutilans with ichthyosis syndrome Finding site Skin structure of sole of foot false Inferred relationship Existential restriction modifier 4
Keratoderma hereditarium mutilans with ichthyosis syndrome Interprets Keratinization, function false Inferred relationship Existential restriction modifier 4
Keratoderma hereditarium mutilans with ichthyosis syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 5
Keratoderma hereditarium mutilans with ichthyosis syndrome Finding site Skin structure of palmar area of hand true Inferred relationship Existential restriction modifier 5
Keratoderma hereditarium mutilans with ichthyosis syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 6
Keratoderma hereditarium mutilans with ichthyosis syndrome Finding site Skin structure of sole of foot true Inferred relationship Existential restriction modifier 6
Keratoderma hereditarium mutilans with ichthyosis syndrome Is a Mutilating keratoderma true Inferred relationship Existential restriction modifier
Keratoderma hereditarium mutilans with ichthyosis syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 4
Keratoderma hereditarium mutilans with ichthyosis syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 4
Keratoderma hereditarium mutilans with ichthyosis syndrome Finding site Structure of auditory system true Inferred relationship Existential restriction modifier 3
Keratoderma hereditarium mutilans with ichthyosis syndrome Is a Congenital keratoderma true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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