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

Back to Browse

Relationship Network

Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.

Click a node to open it in a new tab
Disease: 1Formula: 6Herb: 4Symptom: 3Target: 21Links: 37
Arranging relationship network...

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