DiseaseID 14042

范可尼贫血 N 互补组

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: 17Links: 24
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Record Fields

Scalar fields from the final disease record.

Disease Id
14042
Core Entity Id
71771
Source Entity Count
1
Preferred Name
Fanconi Anemia, Complementation Group N
Name Cn
范可尼贫血 N 互补组
Name Pinyin
Fan Ke Ni Pin Xue n Hu Bu Zu
Name En
Fanconi Anemia, Complementation Group N
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
Version
v1
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Fanconi Anemia, Complementation Group N
Role
preferred
Name
FANCN
Role
alias
Name
Fanconi Anemia Complementation Group N
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS015349
Omim
610832
Umls
C1835817
Sym Map
SMDE00620
Do Class
DOID:630DOID:7
Dis Ge Net
C1835817
Umls Sty
T047
Me Sh Class
C15C16C18
Etcm Disease
Fanconi Anemia, Complementation Group N
Tcmbank Disease
11164
Itcmdb Generated
ITX-DISEASE-C753C63DB85E

Attributes

Merged source attributes and domain-specific metadata.

Version
v1
Suppress
0
Page Title
Disease Fanconi Anemia, Complementation Group N 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 N
Global Category
Cancer diseases;Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Blood diseases;Bone diseases;Immune diseases;Nephrological diseases;Skin diseases
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