Slot: pp_cr7640_familial_cancer_syndrome_subsidiary_comment¶

Specifies or describes familial cancer syndrome where Familial Cancer Syndrome is coded as "Yes" or "Possible". (For example "Li-Fraumeni", "Rhabdoid tumour predisposition syndrome" or "Biallelic PMS2 mutation" to identify distinct syndromes which may have different treatment decisions or outcomes but cannot be coded separately.)

URI: cosd:pp_cr7640_familial_cancer_syndrome_subsidiary_comment

Applicable Classes¶

Name	Description	Modifies Slot
COSDResearchView	Flat research view combining file metadata, patient demographics, primary pat...	no

Properties¶

Type and Range¶

Property	Value
Range	String
Domain Of	COSDResearchView

Cardinality and Requirements¶

Property	Value

Identifier and Mapping Information¶

Annotations¶

property	value
sql_column	PP_CR7640_FAMILIAL_CANCER_SYNDROME_SUBSIDIARY_COMMENT
sql_type	VARCHAR(50)

Schema Source¶

from schema: https://health-informatics-uon.github.io/nuh-data/datasets/cosd

Mappings¶

Mapping Type	Mapped Value
self	cosd:pp_cr7640_familial_cancer_syndrome_subsidiary_comment
native	cosd:pp_cr7640_familial_cancer_syndrome_subsidiary_comment

LinkML Source¶

name: pp_cr7640_familial_cancer_syndrome_subsidiary_comment
annotations:
  sql_column:
    tag: sql_column
    value: PP_CR7640_FAMILIAL_CANCER_SYNDROME_SUBSIDIARY_COMMENT
  sql_type:
    tag: sql_type
    value: VARCHAR(50)
description: Specifies or describes familial cancer syndrome where Familial Cancer
  Syndrome is coded as "Yes" or "Possible". (For example "Li-Fraumeni", "Rhabdoid
  tumour predisposition syndrome" or "Biallelic PMS2 mutation" to identify distinct
  syndromes which may have different treatment decisions or outcomes but cannot be
  coded separately.)
from_schema: https://health-informatics-uon.github.io/nuh-data/datasets/cosd
rank: 1000
domain_of:
- COSDResearchView
range: string
required: false