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717183001: Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3308613015 Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3308614014 Keratoderma hereditarium mutilans with ichthyosis syndrome en Synonym Active Case insensitive SNOMED CT core
3308615010 Camisa disease en Synonym Active Case sensitive SNOMED CT core
3308616011 Keratoderma ichthyosiform dermatosis elevated beta-glucuronidase syndrome en Synonym Active Case insensitive SNOMED CT core
3308617019 Vohwinkel ichthyosis syndrome en Synonym Active Case sensitive SNOMED CT core
3308618012 A diffuse palmoplantar keratoderma with manifestation of honeycomb palmoplantar hyperkeratosis associated with pseudoainhum of the fifth digit of the hand, ichthyosis and deafness.Follows an autosomal dominant mode of transmission. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


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

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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