DiseaseID 6096
色素减退性疾病
disease
NCI2016_NICHD_1602D:A condition characterized by an abnormal loss of color to the skin due to the depletion of melanocytes or melanin.|NCI2016_CTCAE_1602D:A disorder characterized by loss of skin pigment.|NCI2016_02D:Abn
Relationship Network
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Disease: 1Symptom: 3Target: 12Links: 15
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 6096
- Core Entity Id
- 62697
- Source Entity Count
- 1
- Preferred Name
- Hypopigmentation Disorder
- Name Cn
- 色素减退性疾病
- Name Pinyin
- Se Su Jian Tui Xing Ji Bing
- Name En
- Hypopigmentation Disorder
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Skin and Connective Tissue Diseases
- Do Class
- Hpo Class
- Abnormality of the integument
- Mesh Class Name
- Skin and Connective Tissue Diseases
- Hpo Class Name
- Abnormality of the integument
- Do Class Name
- Disease Definition
- NCI2016_NICHD_1602D:A condition characterized by an abnormal loss of color to the skin due to the depletion of melanocytes or melanin.|NCI2016_CTCAE_1602D:A disorder characterized by loss of skin pigment.|NCI2016_02D:Abnormal lightening of skin due to decreased melanin production or deposition. Vitiligo, albinism, and leukoderma are among the disorders that are associated with skin hypopigmentation.|MSH2017_2016_08_12:A condition caused by a deficiency or a loss of melanin pigmentation in the epidermis, also known as hypomelanosis. Hypopigmentation can be localized or generalized, and may result from genetic defects, trauma, inflammation, or infections.|HPO2016_07_04:A reduction of skin color related to a decrease in melanin production and deposition. [HPO:probinson]
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hypopigmentation Disorder
Role
preferred
Name
Hypopigmentation
Role
alias
Name
Hypopigmentation of The Skin
Role
alias
Name
Hypopigmented Skin
Role
alias
Name
Patchy Lightened Skin
Role
alias
Name
Skin Hypopigmentation
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0001010
Herb
HBDIS004165
Me Sh
D017496
Umls
C0162835
Sym Map
SMDE09717
Dis Ge Net
C0162835
Umls Sty
T047
Hpo Class
HP:0001574
Me Sh Class
C17
Tcmbank Disease
15543
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
disease
Hpo Class Name
Abnormality of the integument
Hpo Disease Class
Abnormality of the integument
Umls Disease Type
Disease or Syndrome
Disease Definition
NCI2016_NICHD_1602D:A condition characterized by an abnormal loss of color to the skin due to the depletion of melanocytes or melanin.|NCI2016_CTCAE_1602D:A disorder characterized by loss of skin pigment.|NCI2016_02D:Abnormal lightening of skin due to decreased melanin production or deposition. Vitiligo, albinism, and leukoderma are among the disorders that are associated with skin hypopigmentation.|MSH2017_2016_08_12:A condition caused by a deficiency or a loss of melanin pigmentation in the epidermis, also known as hypomelanosis. Hypopigmentation can be localized or generalized, and may result from genetic defects, trauma, inflammation, or infections.|HPO2016_07_04:A reduction of skin color related to a decrease in melanin production and deposition. [HPO:probinson]
Me Sh Disease Class
Skin and Connective Tissue Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Skin and Connective Tissue Diseases
Umls Semantic Type Name
Disease or Syndrome