DiseaseID 14289
范可尼贫血D1互补组
disease
NCI2016_02D:Fanconi anemia caused by mutations of the BRCA2 gene.
Relationship Network
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Disease: 1Target: 16Links: 24
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 14289
- Core Entity Id
- 72054
- Source Entity Count
- 1
- Preferred Name
- Fanconi Anemia, Complementation Group D1
- Name Cn
- 范可尼贫血D1互补组
- Name Pinyin
- Fan Ke Ni Pin Xue D1 Hu Bu Zu
- Name En
- Fanconi Anemia, Complementation Group D1
- 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 BRCA2 gene.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Fanconi Anemia, Complementation Group D1
Role
preferred
Name
FAD1
Role
alias
Name
FANCD1
Role
alias
Name
Fanconi Anemia Complementation Group D1
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS015681
Omim
605724
Umls
C1838457
Sym Map
SMDE01717
Do Class
DOID:630DOID:7
Dis Ge Net
C1838457
Umls Sty
T047
Me Sh Class
C15C16C18
Etcm Disease
Fanconi Anemia, Complementation Group D1
Tcmbank Disease
3202
Itcmdb Generated
ITX-DISEASE-2C277A56F5D8
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Fanconi Anemia, Complementation Group D1 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 D1
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 BRCA2 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