ITCMDBv1
DiseaseID 2405

泛发性色素异常症

disease

Acropigmentation of Dohi is a genodermatosis characterised by the presence of hyperpigmented and hypopigmented macules, principally located on the extremities and limbs.

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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: 1Formula: 11Herb: 12Symptom: 2Target: 21Links: 49
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Record Fields

Scalar fields from the final disease record.

Disease Id
2405
Core Entity Id
2711
Source Entity Count
1
Preferred Name
Dyschromatosis Universalis
Name Cn
泛发性色素异常症
Name Pinyin
Fan Fa Xing Se Su Yi Chang Zheng
Name En
Dyschromatosis Universalis
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disgenet Type
disease
Mesh Class
Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and Symptoms
Do Class
disease of anatomical entity
Hpo Class
Mesh Class Name
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Hpo Class Name
Do Class Name
disease of anatomical entity
Disease Definition
Acropigmentation of Dohi is a genodermatosis characterised by the presence of hyperpigmented and hypopigmented macules, principally located on the extremities and limbs.
Version
v1
Suppressed
No

Names

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

Name
Dyschromatosis Universalis
Role
preferred
Name
Dyschromatosis Universalis Hereditaria
Role
preferred
Name
Dyschromatosis Universalis Hereditaria 3
Role
preferred
Name
Dyschromatosis Symmetrica Hereditaria
Role
preferred
Name
Dyschromatosis Universalis Hereditaria 1
Role
preferred
Name
Dyschromatosis Universalis Hereditaria 2
Role
preferred
Name
DUH3
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Herb
HBDIS013430HBDIS019405HBDIS020186HBDIS022343HBDIS029112
Omim
615402
Umls
C0406775C1306229C2930995C3809394
Icd10
L81.8
Sym Map
SMDE04840SMDE04979SMDE05118
Do Class
DOID:7
Dis Ge Net
C1306229C2675183C2675711C2930995C3809394
Orphanet
24141
Umls Sty
T047
Me Sh Class
C16C17C23
Etcm Disease
Dyschromatosis Symmetrica HereditariaDyschromatosis Universalis HereditariaDyschromatosis Universalis Hereditaria 1Dyschromatosis Universalis Hereditaria 2Dyschromatosis Universalis Hereditaria 3
Tcmbank Disease
12450166421669629619
Itcmdb Generated
ITX-DISEASE-2E448578FD7CITX-DISEASE-3E762340ED84ITX-DISEASE-75A49EB27185ITX-DISEASE-77A191FD67BFITX-DISEASE-DBECAEC0A186

Attributes

Merged source attributes and domain-specific metadata.

Version
v1v1,v2
Suppress
0
Page Title
Disease Dyschromatosis Symmetrica Hereditaria Details pageDisease Dyschromatosis Universalis Hereditaria 1 Details pageDisease Dyschromatosis Universalis Hereditaria 2 Details pageDisease Dyschromatosis Universalis Hereditaria 3 Details pageDisease Dyschromatosis Universalis Hereditaria Details page
Do Class Name
disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Dyschromatosis Symmetrica Hereditaria
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Skin diseases
Disease Name
Dyschromatosis Universalis Hereditaria
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Neuronal diseases;Skin diseases
Disease Name
Dyschromatosis Universalis Hereditaria 1
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Neuronal diseases;Skin diseases
Disease Name
Dyschromatosis Universalis Hereditaria 2
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Neuronal diseases;Skin diseases
Disease Name
Dyschromatosis Universalis Hereditaria 3
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Neuronal diseases;Skin diseases
Disease Definition
Acropigmentation of Dohi is a genodermatosis characterised by the presence of hyperpigmented and hypopigmented macules, principally located on the extremities and limbs.
Me Sh Disease Class
Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and Symptoms
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
Umls Semantic Type Name
Disease or Syndrome