DiseaseID 8286
全色盲1型
disease
HPO2016_07_04:A condition where the retina contains no functional cone cells, so that in addition to the absence of color discrimination, vision in lights of normal intensity is difficult. [DDD:gblack]
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 1Target: 12Links: 13
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 8286
- Core Entity Id
- 65202
- Source Entity Count
- 1
- Preferred Name
- Achromatopsia 1
- Name Cn
- 全色盲1型
- Name Pinyin
- Quan Se Mang 1 Xing
- Name En
- Achromatopsia 1
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
- Do Class
- Hpo Class
- Abnormality of the eye
- Mesh Class Name
- Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
- Hpo Class Name
- Abnormality of the eye
- Do Class Name
- Disease Definition
- HPO2016_07_04:A condition where the retina contains no functional cone cells, so that in addition to the absence of color discrimination, vision in lights of normal intensity is difficult. [DDD:gblack]
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Achromatopsia 1
Role
preferred
Name
Achromatopsia
Role
alias
Name
Rod Monochromacy
Role
alias
Name
Rod Monochromatism
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0011516
Herb
HBDIS007274
Umls
C0302129
Sym Map
SMDE05331
Dis Ge Net
C0302129
Umls Sty
T047
Hpo Class
HP:0000478
Me Sh Class
C10C11C23
Tcmbank Disease
1509
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
disease
Hpo Class Name
Abnormality of the eye
Hpo Disease Class
Abnormality of the eye
Umls Disease Type
Disease or Syndrome
Disease Definition
HPO2016_07_04:A condition where the retina contains no functional cone cells, so that in addition to the absence of color discrimination, vision in lights of normal intensity is difficult. [DDD:gblack]
Me Sh Disease Class
Eye Diseases; Nervous System Diseases; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome