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Class: PhenotypeDisease

Association between a Human Phenotype Ontology term and a Disease Ontology term identifying a disease especially relevant to it

URI: cfde_schema:PhenotypeDisease

classDiagram class PhenotypeDisease PhenotypeDisease : disease PhenotypeDisease : phenotype

Slots

Name Range Cardinality Description Info
phenotype Phenotype 1..1 A Human Phenotype Ontology CV term ID .
disease Disease 1..1 A Disease Ontology CV term ID .

Usages

Identifier and Mapping Information

Schema Source

  • from schema: https://w3id.org/linkml/cfde

Mappings

Mapping Type Mapped Value
self ['cfde_schema:PhenotypeDisease']
native ['cfde_schema:PhenotypeDisease']

LinkML Specification

Direct

name: phenotype_disease
description: Association between a Human Phenotype Ontology term and a Disease Ontology
  term identifying a disease especially relevant to it
title: phenotype_disease
from_schema: https://w3id.org/linkml/cfde
attributes:
  phenotype:
    name: phenotype
    description: A Human Phenotype Ontology CV term ID
    from_schema: https://w3id.org/linkml/cfde
    range: phenotype
    required: true
  disease:
    name: disease
    description: A Disease Ontology CV term ID
    from_schema: https://w3id.org/linkml/cfde
    range: disease
    required: true
unique_keys:
  phenotype_disease_primary_key:
    unique_key_name: phenotype_disease_primary_key
    unique_key_slots:
    - '[''phenotype'', ''disease'']'

Induced

name: phenotype_disease
description: Association between a Human Phenotype Ontology term and a Disease Ontology
  term identifying a disease especially relevant to it
title: phenotype_disease
from_schema: https://w3id.org/linkml/cfde
attributes:
  phenotype:
    name: phenotype
    description: A Human Phenotype Ontology CV term ID
    from_schema: https://w3id.org/linkml/cfde
    alias: phenotype
    owner: phenotype_disease
    range: phenotype
    required: true
  disease:
    name: disease
    description: A Disease Ontology CV term ID
    from_schema: https://w3id.org/linkml/cfde
    alias: disease
    owner: phenotype_disease
    range: disease
    required: true
unique_keys:
  phenotype_disease_primary_key:
    unique_key_name: phenotype_disease_primary_key
    unique_key_slots:
    - '[''phenotype'', ''disease'']'