DiseaseID 3920
大疱性表皮松解症
disease
NCI2016_NCI-GLOSS_1602D:A group of chronic skin disorders in which fluid-filled blisters form on the skin and mucosa (the moist, inner lining of some organs and body cavities). Epidermolysis bullosa is inherited and usua
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
Click a node to open it in a new tab
Disease: 1Symptom: 4Target: 12Links: 16
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3920
- Core Entity Id
- 60190
- Source Entity Count
- 2
- Preferred Name
- Epidermolysis Bullosa
- Name Cn
- 大疱性表皮松解症
- Name Pinyin
- Da Pao Xing Biao Pi Song Jie Zheng
- Name En
- Epidermolysis Bullosa
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Do Class
- disease of anatomical entity
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity
- Disease Definition
- NCI2016_NCI-GLOSS_1602D:A group of chronic skin disorders in which fluid-filled blisters form on the skin and mucosa (the moist, inner lining of some organs and body cavities). Epidermolysis bullosa is inherited and usually starts at birth. Patients with epidermolysis bullosa may be at increased risk of squamous cell cancer of the skin.|NCI2016_02D:An autosomal recessive inherited skin disorder caused by mutations in the genes encoding keratins 5 and 14, collagen VII or laminin 5. It is characterized by skin fragility and the formation of blisters. The blisters may become large and ulcerated, resulting in skin infections and loss of body fluids.|MSH2017_2016_08_12:Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties.|CSP2006:inherited chronic noninflammatory skin disease manifested by vesicles, large bullae (blisters), and skin erosions which often result from trauma.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Epidermolysis Bullosa
Role
preferred
Name
Epidermolysis Bullosa, Unspecified
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS000952
Me Sh
D004820
Umls
C0014527
Icd10
Q81Q81.9
Sym Map
SMDE08362
Do Class
DOID:7
Dis Ge Net
C0014527
Umls Sty
T019
Me Sh Class
C16C17
Tcmbank Disease
1565916216
Itcmdb Generated
ITX-DISEASE-9A5BABE4AEEF
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity
Umls Disease Type
Congenital Abnormality
Disease Definition
NCI2016_NCI-GLOSS_1602D:A group of chronic skin disorders in which fluid-filled blisters form on the skin and mucosa (the moist, inner lining of some organs and body cavities). Epidermolysis bullosa is inherited and usually starts at birth. Patients with epidermolysis bullosa may be at increased risk of squamous cell cancer of the skin.|NCI2016_02D:An autosomal recessive inherited skin disorder caused by mutations in the genes encoding keratins 5 and 14, collagen VII or laminin 5. It is characterized by skin fragility and the formation of blisters. The blisters may become large and ulcerated, resulting in skin infections and loss of body fluids.|MSH2017_2016_08_12:Group of genetically determined disorders characterized by the blistering of skin and mucosae. There are four major forms: acquired, simple, junctional, and dystrophic. Each of the latter three has several varieties.|CSP2006:inherited chronic noninflammatory skin disease manifested by vesicles, large bullae (blisters), and skin erosions which often result from trauma.
Me Sh Disease Class
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
Umls Semantic Type Name
Congenital Abnormality