FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

717228004: Hereditary palmoplantar keratoderma Gamborg Nielsen type (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
3308744016 Hereditary palmoplantar keratoderma Gamborg Nielsen type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3308745015 Hereditary palmoplantar keratoderma Gamborg Nielsen type en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hereditary palmoplantar keratoderma Gamborg Nielsen type Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Hereditary palmoplantar keratoderma Gamborg Nielsen type Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
Hereditary palmoplantar keratoderma Gamborg Nielsen type Is a Hereditary diffuse palmoplantar keratoderma true Inferred relationship Existential restriction modifier
Hereditary palmoplantar keratoderma Gamborg Nielsen type Has definitional manifestation Abnormal keratinization false Inferred relationship Existential restriction modifier
Hereditary palmoplantar keratoderma Gamborg Nielsen type Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Hereditary palmoplantar keratoderma Gamborg Nielsen type Finding site Skin structure false Inferred relationship Existential restriction modifier 4
Hereditary palmoplantar keratoderma Gamborg Nielsen type Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Hereditary palmoplantar keratoderma Gamborg Nielsen type Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Hereditary palmoplantar keratoderma Gamborg Nielsen type Associated morphology Hyperkeratosis false Inferred relationship Existential restriction modifier 4
Hereditary palmoplantar keratoderma Gamborg Nielsen type Has interpretation Abnormal false Inferred relationship Existential restriction modifier 1
Hereditary palmoplantar keratoderma Gamborg Nielsen type Interprets Keratinization, function false Inferred relationship Existential restriction modifier 1
Hereditary palmoplantar keratoderma Gamborg Nielsen type Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 2
Hereditary palmoplantar keratoderma Gamborg Nielsen type Associated morphology Hyperkeratosis true Inferred relationship Existential restriction modifier 1
Hereditary palmoplantar keratoderma Gamborg Nielsen type Finding site Skin structure of sole of foot false Inferred relationship Existential restriction modifier 1
Hereditary palmoplantar keratoderma Gamborg Nielsen type Finding site Skin structure of palmar area of hand false Inferred relationship Existential restriction modifier 2
Hereditary palmoplantar keratoderma Gamborg Nielsen type Finding site Entire skin of palmar area of hand true Inferred relationship Existential restriction modifier 1
Hereditary palmoplantar keratoderma Gamborg Nielsen type Finding site Entire skin of sole of foot true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

Back to Start