DiseaseID 3787
婴儿湿疹
disease
MSH2017_2016_08_12:A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposi
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Experiment: 3Formula: 10Herb: 12Symptom: 12Target: 24Links: 61
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3787
- Core Entity Id
- 60036
- Source Entity Count
- 1
- Preferred Name
- Eczema, Infantile
- Name Cn
- 婴儿湿疹
- Name Pinyin
- Ying Er Shi Zhen
- Name En
- Eczema, Infantile
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Immune System Diseases; Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Do Class
- disease of anatomical entity
- Hpo Class
- Abnormality of the immune system; Abnormality of the integument
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases
- Hpo Class Name
- Abnormality of the integument; Abnormality of the immune system
- Do Class Name
- disease of anatomical entity
- Disease Definition
- MSH2017_2016_08_12:A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema.|HPO2016_07_04:A chronic inflammatory genetically determined disease of the skin manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. [HPO:probinson]|CSP2006:chronic inflammatory skin disorder in individuals with a hereditary predisposition to a lowered threshold to pruritus; characterized by extreme itching, leading to scratching and rubbing that result in typical lesions of eczema.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Eczema, Infantile
Role
preferred
Name
Dermatitis, Atopic
Role
preferred
Name
Atopic Dermatitis
Role
alias
Name
Atopic Dermatitis, Chronic
Role
alias
Name
Atopic Dermatitis, Unspecified
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0001047
Herb
HBDIS000761HBDIS003389
Me Sh
D003876
Umls
C0011615C0086196
Icd10
L20L20.81L20.9
Sym Map
SMDE07818SMDE08163
Do Class
DOID:7
Dis Ge Net
C0011615C0086196
Umls Sty
T047
Hpo Class
HP:0001574HP:0002715
Me Sh Class
C16C17C20
Etcm Disease
Dermatitis, Atopic
Tcmbank Disease
15987208816192
Itcmdb Generated
ITX-DISEASE-7BB97C14B49BITX-DISEASE-9164E5C0D8F0ITX-DISEASE-E612B1CFF12B
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Page Title
Disease Dermatitis, Atopic Details page
Do Class Name
disease of anatomical entity
Disease Type
disease
Hpo Class Name
Abnormality of the integument; Abnormality of the immune system
Do Disease Class
disease of anatomical entity
Hpo Disease Class
Abnormality of the immune system; Abnormality of the integument
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Dermatitis, Atopic
Global Category
Genetic diseases
Anatomical Category
Immune diseases;Neuronal diseases;Skin diseases
Disease Definition
MSH2017_2016_08_12:A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema.|HPO2016_07_04:A chronic inflammatory genetically determined disease of the skin manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. [HPO:probinson]|CSP2006:chronic inflammatory skin disorder in individuals with a hereditary predisposition to a lowered threshold to pruritus; characterized by extreme itching, leading to scratching and rubbing that result in typical lesions of eczema.
Me Sh Disease Class
Immune System Diseases; Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Immune System Diseases
Umls Semantic Type Name
Disease or Syndrome