Preferred Label : linked gene;
Origin ID : F-E0370;
UMLS CUI : C0314613;
Automatic exact mappings (from CISMeF team)
- Currated CISMeF NLP mapping
- SNOMED CT concept
- Semantic type(s)
- UMLS correspondences (same concept)
http://www.sudoc.abes.fr/cbs/xslt//DB=2.1/SET=1/TTL=115/(prochainement%20disponible)
2021
France
dissertations, academic
Literature
phenotype
disease
phenotype
genotype
Pathology
Pathology
Pathology
multigene family
gene clusters
genetic association studies
genotype
persons
Pathology
linked gene
Pathology
Disorders
Pathology
Pathology
review literature as topic
phenotype
genotype
---
https://www.snfge.org/sites/www.snfge.org/files/medias/documents/Fiche%20GENMAD_Conseils%20de%20prise%20en%20charge%20de%20la%20maladie%20de%20la%20polypose%20familiale%20lie%CC%81e%20au%20ge%CC%80ne%20APC_2021.pdf
2021
France
guideline
disease management
linked gene
APC Gene
Embarrassed by Illness
familial disease, nos
Charge
Familial Adenomatous Polyposis
counseling
multiple polyps
Transjugular Intrahepatic Portosystemic Shunt
genes, apc
---
https://anpgm.fr/media/documents/anpgm_047_v3_syndrome_de_lx_fragile.pdf
2018
France
guideline
tremor, nos
primary ovarian insufficiency
fragile x syndrome
ataxia, nos
infant, premature
tremor
due to
Tremor
immature
ataxia
fragile X tremor ataxia syndrome
ovary, nos
Ataxia
insufficiency
linked gene
Ovarian failure
genes, vif
infant, premature
---
https://anpgm.fr/media/documents/ANPGM_064_Retard_mental_et_deficit_en_GH_SOX3.doc
2009
France
guideline
deficiency, mental
genes, x-linked
linked gene
X-Linked Intellectual Disability
abnormal mental state
intellectual disability
---
https://anpgm.fr/media/documents/ANPGM_052_Lissencephalie_LIS1_et_DCX.doc
2009
France
guideline
genes
lissencephaly
Lissencephaly
linked gene
---
https://anpgm.fr/media/documents/ANPGM_053_RM_li_au_gne_Oligophrnine.doc
2009
France
guideline
mental retardation
intellectual disability
Embarrassment
genes
mental retardation, nos
linked gene
---
