DiseaseID 6957
假性痛风
disease
Familial calcium pyrophosphate deposition (CPPD) is a chronic inherited arthropathy characterized by chondrocalcinosis (CC; i.e. cartilage calcification), often associated with recurrent acute calcium
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Disease: 1Formula: 3Symptom: 9Target: 23Links: 36
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 6957
- Core Entity Id
- 63679
- Source Entity Count
- 1
- Preferred Name
- Pseudogout
- Name Cn
- 假性痛风
- Name Pinyin
- Jia Xing Tong Feng
- Name En
- Pseudogout
- 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; Musculoskeletal DiseasesMusculoskeletal DiseasesNutritional and Metabolic Diseases; Musculoskeletal Diseases
- Do Class
- disease of anatomical entitygenetic disease; disease of anatomical entity; disease of metabolismgenetic disease; disease of metabolism
- Hpo Class
- Abnormality of connective tissue; Abnormality of the skeletal system
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal DiseasesMusculoskeletal DiseasesNutritional and Metabolic Diseases; Musculoskeletal Diseases
- Hpo Class Name
- Abnormality of the skeletal system; Abnormality of connective tissue
- Do Class Name
- disease of anatomical entitydisease of metabolism; genetic diseasedisease of metabolism; genetic disease; disease of anatomical entity
- Disease Definition
- Familial calcium pyrophosphate deposition (CPPD) is a chronic inherited arthropathy characterized by chondrocalcinosis (CC; i.e. cartilage calcification), often associated with recurrent acute calcium
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Pseudogout
Role
preferred
Name
Calcium Pyrophosphate Deposition Disease
Role
preferred
Name
Calcium Pyrophosphate Dihydrate Deposition
Role
preferred
Name
Calcium Pyrophosphate Arthropathy
Role
preferred
Name
Familial Calcium Pyrophosphate Deposition
Role
preferred
Name
Familial Chondrocalcinosis
Role
preferred
Name
Other Chondrocalcinosis
Role
preferred
Name
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL
Role
preferred
Name
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 1
Role
preferred
Name
Calcium Deposits In Joints
Role
alias
Name
Chondrocalcinosis
Role
alias
Name
Chondrocalcinosis 2
Role
alias
Name
Hyperphosphatemic Familial Tumoral Calcinosis
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0000934
Herb
HBDIS002506HBDIS005402HBDIS009020HBDIS009706HBDIS010173HBDIS012049HBDIS018515HBDIS027519
Me Sh
D002805
Omim
118600211900
Umls
C0242217C0553730C0856830
Icd10
M11.1M11.2
Sym Map
SMDE02519SMDE06697SMDE06698
Do Class
DOID:0014667DOID:630DOID:7
Dis Ge Net
C0033802C0242217C0409896C0477548C0553730C0856830C1876187C4692564
Orphanet
1416
Umls Sty
T047
Hpo Class
HP:0000924HP:0003549
Me Sh Class
C05C16C18
Etcm Disease
Familial Calcium Pyrophosphate Deposition
Tcmbank Disease
104791221517006176242884530201317115434
Itcmdb Generated
ITX-DISEASE-C3BDB3CE6C31ITX-DISEASE-F906C42FA38A
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v2
Suppress
0
Page Title
Disease Familial Calcium Pyrophosphate Deposition Details page
Do Class Name
disease of anatomical entitydisease of metabolism; genetic diseasedisease of metabolism; genetic disease; disease of anatomical entity
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of the skeletal system; Abnormality of connective tissue
Do Disease Class
disease of anatomical entitygenetic disease; disease of anatomical entity; disease of metabolismgenetic disease; disease of metabolism
Hpo Disease Class
Abnormality of connective tissue; Abnormality of the skeletal system
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Familial Calcium Pyrophosphate Deposition
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Bone diseases
Disease Definition
Familial calcium pyrophosphate deposition (CPPD) is a chronic inherited arthropathy characterized by chondrocalcinosis (CC; i.e. cartilage calcification), often associated with recurrent acute calciumMSH2017_2016_08_12:Presence of CALCIUM PYROPHOSPHATE in the connective tissues such as the cartilaginous structures of joints. When accompanied by GOUT-like symptoms, it is referred to as pseudogout.|HPO2016_07_04:Radiographic evidence of articular calcification that represent calcium pyrophosphate depositions in soft tissue surrounding joints and at the insertions of tendons near joints (Entheses/Sharpey fibers) . [HPO:sdoelken]
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal DiseasesMusculoskeletal DiseasesNutritional and Metabolic Diseases; Musculoskeletal Diseases
Dis Ge Net Disease Type
diseasephenotype
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Musculoskeletal DiseasesMusculoskeletal DiseasesNutritional and Metabolic Diseases; Musculoskeletal Diseases
Umls Semantic Type Name
Disease or Syndrome