Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 1Target: 16Links: 25
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 18149
- Core Entity Id
- 76501
- Source Entity Count
- 1
- Preferred Name
- Fanconi Anemia, Complementation Group L
- Name Cn
- 范可尼贫血互补L组
- Name Pinyin
- Fan Ke Ni Pin Xue Hu Bu L Zu
- Name En
- Fanconi Anemia, Complementation Group L
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Mesh Class Name
- Hpo Class Name
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Fanconi Anemia, Complementation Group L
Role
preferred
Name
FANCL
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS021417
Omim
614083
Umls
C3469528
Sym Map
SMDE01417
Do Class
DOID:630DOID:7
Dis Ge Net
C3469528
Umls Sty
T047
Etcm Disease
Fanconi Anemia, Complementation Group L
Tcmbank Disease
16497
Itcmdb Generated
ITX-DISEASE-86FFB9FCAC11
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Page Title
Disease Fanconi Anemia, Complementation Group L 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 L
Global Category
Cancer diseases;Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Bone diseases;Immune diseases;Nephrological diseases;Skin diseases
Dis Ge Net Disease Type
disease
Umls Semantic Type Name
Disease or Syndrome