DiseaseID 17683

范可尼贫血互补群O

disease

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Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

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Disease: 1Target: 18Links: 24
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Record Fields

Scalar fields from the final disease record.

Disease Id
17683
Core Entity Id
75958
Source Entity Count
1
Preferred Name
Fanconi Anemia, Complementation Group O
Name Cn
范可尼贫血互补群O
Name Pinyin
Fan Ke Ni Pin Xue Hu Bu Qun O
Name En
Fanconi Anemia, Complementation Group O
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 O
Role
preferred
Name
FANCO
Role
alias
Name
Fanconi Anemia Complementation Group O
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS020648
Omim
613390
Umls
C3150653
Sym Map
SMDE04576
Do Class
DOID:630DOID:7
Dis Ge Net
C3150653
Umls Sty
T047
Etcm Disease
Fanconi Anemia, Complementation Group O
Tcmbank Disease
24471
Itcmdb Generated
ITX-DISEASE-997194C67405

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Fanconi Anemia, Complementation Group O 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 O
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