DiseaseID 9881
布鲁克综合征
disease
Arthrogryposis-like syndrome, also known as Kuskokwim disease, is a very rare congenital contracture disorder, reported exclusively in Yup'ik Eskimos of the Kuskokwim River delta region of Alaska, cha
Relationship Network
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Disease: 1Formula: 6Herb: 4Symptom: 3Target: 21Links: 37
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 9881
- Core Entity Id
- 67014
- Source Entity Count
- 1
- Preferred Name
- Bruck Syndrome
- Name Cn
- 布鲁克综合征
- Name Pinyin
- Bu Lu Ke Zong He Zheng
- Name En
- Bruck Syndrome
- 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; Musculoskeletal DiseasesSkin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
- Do Class
- syndrome
- Hpo Class
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
- Hpo Class Name
- Do Class Name
- syndrome
- Disease Definition
- Arthrogryposis-like syndrome, also known as Kuskokwim disease, is a very rare congenital contracture disorder, reported exclusively in Yup'ik Eskimos of the Kuskokwim River delta region of Alaska, cha
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Bruck Syndrome
Role
preferred
Name
Arthrogryposis-Like Syndrome
Role
preferred
Name
Bruck Syndrome 1
Role
preferred
Name
Bruck Syndrome 2
Role
preferred
Name
Kuskokwim Disease
Role
preferred
Name
ARTHROGRYPOSIS-LIKE DISORDER
Role
alias
Name
BRKS1
Role
alias
Name
BRKS2
Role
alias
Name
OSTEOGENESIS IMPERFECTA WITH CONGENITAL JOINT CONTRACTURES
Role
alias
Name
Osteogenesis Imperfecta-congenital Joint Contractures Syndrome
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS009419HBDIS015453HBDIS016686HBDIS017707
Omim
208200609220
Umls
C0432253C1836602C1850168C1859709
Icd10
M21.8
Med Dra
10063718
Sym Map
SMDE00655SMDE02399SMDE02544SMDE03394
Do Class
DOID:225
Dis Ge Net
C0432253C1836602C1850168C1859709
Orphanet
11492771
Umls Sty
T047
Me Sh Class
C05C16C17
Etcm Disease
Bruck SyndromeBruck Syndrome 1Bruck Syndrome 2
Tcmbank Disease
155262925338674232
Itcmdb Generated
ITX-DISEASE-73855506BE25ITX-DISEASE-B611EFD67A42ITX-DISEASE-EC5856154743
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2
Suppress
0
Page Title
Disease Bruck Syndrome 1 Details pageDisease Bruck Syndrome 2 Details pageDisease Bruck Syndrome Details page
Do Class Name
syndrome
Disease Type
disease
Do Disease Class
syndrome
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Bruck Syndrome
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Bone diseases;Oral diseases
Disease Name
Bruck Syndrome 1
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Bone diseases;Oral diseases
Disease Name
Bruck Syndrome 2
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Bone diseases;Oral diseases
Disease Definition
Arthrogryposis-like syndrome, also known as Kuskokwim disease, is a very rare congenital contracture disorder, reported exclusively in Yup'ik Eskimos of the Kuskokwim River delta region of Alaska, chaBruck syndrome is characterised by the association of osteogenesis imperfecta and congenital joint contractures.
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal DiseasesSkin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Skin and Connective Tissue Diseases; Musculoskeletal Diseases
Umls Semantic Type Name
Disease or Syndrome