DiseaseID 7239
神经皮肤综合征
disease
NCI2016_02D:A hereditary syndrome affecting the central nervous system that is associated with lesions of the skin and retina. Representative examples include neurofibromatosis, tuberous sclerosis, von Hippel-Lindau synd
Relationship Network
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Disease: 1Symptom: 5Target: 12Links: 17
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 7239
- Core Entity Id
- 64005
- Source Entity Count
- 1
- Preferred Name
- Neurocutaneous Syndromes
- Name Cn
- 神经皮肤综合征
- Name Pinyin
- Shen Jing Pi Fu Zong He Zheng
- Name En
- Neurocutaneous Syndromes
- 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; Nervous System Diseases
- Do Class
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Nervous System Diseases
- Hpo Class Name
- Do Class Name
- Disease Definition
- NCI2016_02D:A hereditary syndrome affecting the central nervous system that is associated with lesions of the skin and retina. Representative examples include neurofibromatosis, tuberous sclerosis, von Hippel-Lindau syndrome, and Sturge-Weber syndrome.|MSH2017_2016_08_12:A group of disorders characterized by ectodermal-based malformations and neoplastic growths in the skin, nervous system, and other organs.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Neurocutaneous Syndromes
Role
preferred
Name
Phakomatosis, Unspecified
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS005811
Me Sh
D020752
Umls
C0265316
Icd10
Q85.9
Sym Map
SMDE11425
Dis Ge Net
C0265316
Umls Sty
T047
Me Sh Class
C10C16C17
Tcmbank Disease
20217
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
disease
Umls Disease Type
Disease or Syndrome
Disease Definition
NCI2016_02D:A hereditary syndrome affecting the central nervous system that is associated with lesions of the skin and retina. Representative examples include neurofibromatosis, tuberous sclerosis, von Hippel-Lindau syndrome, and Sturge-Weber syndrome.|MSH2017_2016_08_12:A group of disorders characterized by ectodermal-based malformations and neoplastic growths in the skin, nervous system, and other organs.
Me Sh Disease Class
Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Nervous System Diseases
Umls Semantic Type Name
Disease or Syndrome