DiseaseID 18148
范可尼贫血互补G组
disease
NCI2016_02D:Fanconi anemia caused by mutations of the FANCG gene.
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Disease: 1Symptom: 3Target: 17Links: 27
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 18148
- Core Entity Id
- 76500
- Source Entity Count
- 1
- Preferred Name
- Fanconi Anemia Complementation Group G
- Name Cn
- 范可尼贫血互补G组
- Name Pinyin
- Fan Ke Ni Pin Xue Hu Bu G Zu
- Name En
- Fanconi Anemia Complementation Group G
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
- Hpo Class Name
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- NCI2016_02D:Fanconi anemia caused by mutations of the FANCG gene.
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Fanconi Anemia Complementation Group G
Role
preferred
Name
Fanconi Anemia, Complementation Group G
Role
preferred
Name
FANCG
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS021416
Omim
614082
Umls
C3469527
Sym Map
SMDE02222
Do Class
DOID:630DOID:7
Dis Ge Net
C3469527
Umls Sty
T047
Me Sh Class
C15C16C18
Etcm Disease
Fanconi Anemia, Complementation Group G
Tcmbank Disease
18103
Itcmdb Generated
ITX-DISEASE-97FE790CB2E1
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Fanconi Anemia, Complementation Group G Details page
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Fanconi Anemia, Complementation Group G
Global Category
Cancer diseases;Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Bone diseases;Immune diseases;Nephrological diseases;Skin diseases
Disease Definition
NCI2016_02D:Fanconi anemia caused by mutations of the FANCG gene.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or Syndrome