DiseaseID 5455
幼年黄色肉芽肿
disease
NCI2016_02D:A benign histiocytic tumor that occurs during childhood; it is distinct from Langerhans cell histiocytosis. It is characterized by the presence of lipid-laden, foamy histiocytes and Touton-type giant cells in
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Disease: 1Symptom: 7Target: 20Links: 31
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 5455
- Core Entity Id
- 61957
- Source Entity Count
- 1
- Preferred Name
- Juvenile Xanthogranuloma
- Name Cn
- 幼年黄色肉芽肿
- Name Pinyin
- You Nian Huang Se Rou Ya Zhong
- Name En
- Juvenile Xanthogranuloma
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Neoplastic Process
- Disgenet Type
- disease
- Mesh Class
- Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases
- Do Class
- disease of anatomical entity
- Hpo Class
- Mesh Class Name
- Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases
- Hpo Class Name
- Do Class Name
- disease of anatomical entity
- Disease Definition
- NCI2016_02D:A benign histiocytic tumor that occurs during childhood; it is distinct from Langerhans cell histiocytosis. It is characterized by the presence of lipid-laden, foamy histiocytes and Touton-type giant cells in the dermis. The lesions usually develop during infancy. They consist of cutaneous papules and nodules (most often in the head and neck). It is sometimes associated with deep soft tissues nodules.|MSH2017_2016_08_12:Benign disorder of infants and children caused by proliferation of HISTIOCYTES, macrophages found in tissues. These histiocytes, usually lipid-laden non-Langerhans cells, form multiple yellow-red nodules most often in the skin, the eye, and sometimes in the viscera. Patients appear to have normal lipid metabolism and are classified as a normolipemic non-Langerhans cell histiocytosis.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Juvenile Xanthogranuloma
Role
preferred
Name
Xanthogranuloma, Juvenile
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS003156
Me Sh
D014972
Umls
C0043324
Sym Map
SMDE10140
Do Class
DOID:7
Dis Ge Net
C0043324
Umls Sty
T191
Me Sh Class
C15C17
Etcm Disease
Juvenile Xanthogranuloma
Tcmbank Disease
29530
Itcmdb Generated
ITX-DISEASE-3A4088F7ADE7
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Page Title
Disease Juvenile Xanthogranuloma Details page
Do Class Name
disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity
Umls Disease Type
Neoplastic Process
Basic Information
Disease Name
Juvenile Xanthogranuloma
Global Category
Rare diseases
Anatomical Category
Bone diseases;Immune diseases;Skin diseases
Disease Definition
NCI2016_02D:A benign histiocytic tumor that occurs during childhood; it is distinct from Langerhans cell histiocytosis. It is characterized by the presence of lipid-laden, foamy histiocytes and Touton-type giant cells in the dermis. The lesions usually develop during infancy. They consist of cutaneous papules and nodules (most often in the head and neck). It is sometimes associated with deep soft tissues nodules.|MSH2017_2016_08_12:Benign disorder of infants and children caused by proliferation of HISTIOCYTES, macrophages found in tissues. These histiocytes, usually lipid-laden non-Langerhans cells, form multiple yellow-red nodules most often in the skin, the eye, and sometimes in the viscera. Patients appear to have normal lipid metabolism and are classified as a normolipemic non-Langerhans cell histiocytosis.
Me Sh Disease Class
Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Neoplastic Process