DiseaseID 2227

4型全色盲

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: 1Herb: 2Symptom: 3Target: 18Links: 30
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Record Fields

Scalar fields from the final disease record.

Disease Id
2227
Core Entity Id
2506
Source Entity Count
1
Preferred Name
Achromatopsia 4
Name Cn
4型全色盲
Name Pinyin
4 Xing Quan Se Mang
Name En
Achromatopsia 4
Name Latin
Bilingual Status
complete
Disease Type
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Do Class
disease of anatomical entity
Hpo Class
Mesh Class Name
Hpo Class Name
Do Class Name
Disease Definition
Version
v1,v2
Suppressed
No

Names

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

Name
Achromatopsia 4
Role
preferred

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS028834
Omim
613856
Umls
C1841721
Sym Map
SMDE03133
Do Class
DOID:7
Dis Ge Net
C1841721
Umls Sty
T047
Me Sh Class
C10C11C16C23
Etcm Disease
Achromatopsia 4
Itcmdb Generated
ITX-DISEASE-9B235E449CB6

Attributes

Merged source attributes and domain-specific metadata.

Version
v1,v2
Suppress
0
Page Title
Disease Achromatopsia 4 Details page
Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Achromatopsia 4
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Eye diseases
Me Sh Disease Class
Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease