MNDA_FH

Coding system: SNOMED CT (UK Clinical Edition)
Coding system release: unknown
Author: Tom Nichols
Codelist ID: user/tom-nichols/mnda_fh
Version ID: 4259e5f9
Number of codes included: 17

Versions

4b8e15b6 Published
Created: 20 Oct 2022 at 12:33
4259e5f9 Published
Created: 06 Sep 2022 at 16:53

Description

MNDA Positive family history of MND or other neurodegenerative disease

Methodology

I manually reviewed the conditions under the Family History of Neurological Disease hierarchy, finding the relevant pre-coordinated terms. Specialist review exclusions; Family history of childhood convulsion 495171000000108) and inclusions: Family history of disorder of peripheral nervous system(431882002, Family history of Charcot-Marie-Tooth disease(429970002), Family history: Paraplegia(160339007).

Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.

We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.

code	term
160325007	Family history: Senile dementia
160336000	Family history: Huntington's chorea
160337009	Family history: Multiple sclerosis
160344000	Family history: Motor neurone disease
266891008	Family history of central nervous system disorder
275117004	Family history: Parkinsonism
275940001	Family history: Brain disorder
297239000	Family history of neurological disorder
297240003	Family history of Parkinson's disease
394877006	Family history: Alzheimer's disease
429961000	Family history of dementia
430727006	Family history of amyotrophic lateral sclerosis
430809001	Family history of movement disorder
430814002	Family history of neuropathy
433278001	Family history of presenile dementia
495171000000108	Family history of childhood convulsion
98251000119101	Family history of spongy degeneration of central nervous system

This page shows the search terms that were used to build the codelist. Concepts that match the search terms, but which were excluded, are in faint grey.

Family history of hereditary disease

Included 1 out of 29 matching concepts.

Show matching concepts

Family history of Charcot-Marie-Tooth disease (429970002)
Family history of Cowden syndrome (65031000119108)
Family history of Marfan syndrome (64181000119106)
Family history of Tay-Sachs disease (63901000119104)
Family history of Von Hippel-Lindau syndrome (64971000119106)
Family history of achondroplasia (64121000119107)
Family history of alpha thalassemia (64431000119101)
Family history of alpha-1-antitrypsin deficiency (431912005)
Family history of beta thalassemia (64371000119105)
Family history of cystic fibrosis (160309002)
Family history of double heterozygous familial hypercholesterolemia (109271000119105)
Family history of familial dysautonomia (94691000119101)
Family history of familial multiple polyposis syndrome (709090007)
Family history of fragile X syndrome (65071000119106)
Family history of glycogen storage disease (64251000119106)
Family history of hemoglobinopathy E (64391000119106)
Family history of hereditary disease (429962007)
Family history of hereditary nonpolyposis colon cancer (1098871000119109)
Family history of heritable malignancy (81651000119109)
Family history of phenylketonuria (64161000119102)
Family history of retinitis pigmentosa (71271000119107)
Family history of sickle cell anemia (160320002)
Family history of spinocerebellar ataxia (63881000119101)
Family history of tuberous sclerosis (417001009)
Family history: Hereditary spherocytosis (160318000)
Family history: Huntington's chorea (160336000)
Family history: Sickle cell trait (160321003)
Family history: Spherocytosis (308746008)
Family history: Thalassemia (160319008)

Family history of neurological disorder

Included 17 out of 44 matching concepts.