DiseaseID 7000
多发性皮脂腺囊肿
disease
MSH2017_2016_08_12:A disorder characterized by multiple, wide spread cutaneous cysts that often become inflamed and rupture. It is caused by the same mutations in the gene coding for KRT-17 that are causative mutations f
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Disease: 1Target: 6Links: 6
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 7000
- Core Entity Id
- 63730
- Source Entity Count
- 2
- Preferred Name
- Steatocystoma Multiplex
- Name Cn
- 多发性皮脂腺囊肿
- Name Pinyin
- Duo Fa Xing Pi Zhi Xian Nang Zhong
- Name En
- Steatocystoma Multiplex
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Neoplastic Process
- Disgenet Type
- disease
- Mesh Class
- Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Do Class
- Hpo Class
- Neoplasm; Abnormality of the integument
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases
- Hpo Class Name
- Abnormality of the integument; Neoplasm
- Do Class Name
- Disease Definition
- MSH2017_2016_08_12:A disorder characterized by multiple, wide spread cutaneous cysts that often become inflamed and rupture. It is caused by the same mutations in the gene coding for KRT-17 that are causative mutations for Pachyonychia congenita, Type 2. Natal teeth involvement is sometimes associated with steatocystoma multiplex.|HPO2016_07_04:Multiple, localized or widespread, asymptomatic or inflammatory dermal cysts involving the pilosebaceous units. Lesions can appear anywhere on the body, but steatocystoma multiplex is more commonly involved with those areas of the skin with a high density of developed pilosebaceous units (e.g., the axilla, groin, neck, and proximal extremities). [HPO:probinson, pmid:20631281]
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Steatocystoma Multiplex
Role
preferred
Name
Multiplex Steatocystoma
Role
alias
Name
Steatocystoma multiplex
Role
preferred
Source
TCMBank
Preferred
Yes
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0012035
Herb
HBDIS005481
Me Sh
D062685
Omim
184500
Umls
C0259771
Icd10
L72.2
Sym Map
SMDE03193
Dis Ge Net
C0259771
Umls Sty
T191
Hpo Class
HP:0001574HP:0001574;HP:0002664HP:0002664
Me Sh Class
C16C17
Tcmbank Disease
110115744
Itcmdb Generated
ITX-DISEASE-36AAC1D963CE
Attributes
Merged source attributes and domain-specific metadata.
Version
v1
Suppress
0
Disease Type
disease
Hpo Class Name
Abnormality of the integument; Neoplasm
Hpo Disease Class
Neoplasm; Abnormality of the integument
Umls Disease Type
Neoplastic Process
Disease Definition
MSH2017_2016_08_12:A disorder characterized by multiple, wide spread cutaneous cysts that often become inflamed and rupture. It is caused by the same mutations in the gene coding for KRT-17 that are causative mutations for Pachyonychia congenita, Type 2. Natal teeth involvement is sometimes associated with steatocystoma multiplex.|HPO2016_07_04:Multiple, localized or widespread, asymptomatic or inflammatory dermal cysts involving the pilosebaceous units. Lesions can appear anywhere on the body, but steatocystoma multiplex is more commonly involved with those areas of the skin with a high density of developed pilosebaceous units (e.g., the axilla, groin, neck, and proximal extremities). [HPO:probinson, pmid:20631281]
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
Neoplastic Process