Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 7Target: 18Links: 31
Arranging relationship network...
Record Fields
Scalar fields from the final disease record.
- Disease Id
- 14464
- Core Entity Id
- 72253
- Source Entity Count
- 1
- Preferred Name
- Hermansky-Pudlak Syndrome 2
- Name Cn
- Hermansky-Pudlak综合征2型
- Name Pinyin
- Hermansky-pudlak Zong He Zheng 2 Xing
- Name En
- Hermansky-Pudlak Syndrome 2
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases
- Do Class
- genetic disease
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases
- Hpo Class Name
- Do Class Name
- genetic disease
- Disease Definition
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Hermansky-Pudlak Syndrome 2
Role
preferred
Name
HPS2
Role
alias
Name
Hermansky Pudlak Syndrome 2
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS015927
Omim
608233
Umls
C1842362
Sym Map
SMDE01999
Do Class
DOID:630
Dis Ge Net
C1842362
Umls Sty
T047
Me Sh Class
C11C15C16C17C18
Etcm Disease
Hermansky-Pudlak Syndrome 2
Tcmbank Disease
31847
Itcmdb Generated
ITX-DISEASE-9B2EBB3E7BC4
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Hermansky-Pudlak Syndrome 2 Details page
Do Class Name
genetic disease
Disease Type
disease
Do Disease Class
genetic disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Hermansky-Pudlak Syndrome 2
Global Category
Genetic diseases;Metabolic diseases;Rare diseases
Anatomical Category
Blood diseases;Eye diseases;Immune diseases;Neuronal diseases;Skin diseases
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Skin and Connective Tissue Diseases; Hemic and Lymphatic Diseases
Umls Semantic Type Name
Disease or Syndrome