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763775000: Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3643799015 KLICK syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3643800016 Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3643801017 Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Is a Mutilating keratoderma false Inferred relationship Existential restriction modifier
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Is a Autosomal recessive ichthyosis true Inferred relationship Existential restriction modifier
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Has interpretation Abnormal true Inferred relationship Existential restriction modifier 3
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Interprets Keratinization, function true Inferred relationship Existential restriction modifier 3
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 2
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 1
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Finding site Skin structure of palmar area of hand false Inferred relationship Existential restriction modifier 2
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 4
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Is a Erythrokeratodermia variabilis false Inferred relationship Existential restriction modifier
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Finding site Skin structure of sole of foot false Inferred relationship Existential restriction modifier 4
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Finding site Entire skin true Inferred relationship Existential restriction modifier 1
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Is a Hereditary diffuse palmoplantar keratoderma true Inferred relationship Existential restriction modifier
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Is a Rough skin of hands true Inferred relationship Existential restriction modifier
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Finding site Entire skin of palmar area of hand true Inferred relationship Existential restriction modifier 2
Keratosis linearis, ichthyosis congenita, sclerosing keratoderma syndrome Finding site Entire skin of sole of foot true Inferred relationship Existential restriction modifier 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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