DiseaseID 4005
骨化性肌炎
disease
Fibrodysplasia ossificans progressiva (FOP) is a severely disabling heritable disorder of connective tissue characterized by congenital malformations of the great toes and progressive heterotopic ossi
Relationship Network
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Disease: 1Symptom: 11Target: 19Links: 35
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4005
- Core Entity Id
- 60288
- Source Entity Count
- 1
- Preferred Name
- Myositis Ossificans
- Name Cn
- 骨化性肌炎
- Name Pinyin
- Gu Hua Xing Ji Yan
- Name En
- Myositis Ossificans
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Disease or Syndrome
- Disgenet Type
- disease
- Mesh Class
- Musculoskeletal Diseases
- Do Class
- disease of anatomical entity; genetic disease
- Hpo Class
- Mesh Class Name
- Musculoskeletal Diseases
- Hpo Class Name
- Do Class Name
- genetic disease; disease of anatomical entity
- Disease Definition
- Fibrodysplasia ossificans progressiva (FOP) is a severely disabling heritable disorder of connective tissue characterized by congenital malformations of the great toes and progressive heterotopic ossi
- Version
- v1,v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Myositis Ossificans
Role
preferred
Name
Fibrodysplasia Ossificans Progressiva
Role
preferred
Name
FOP
Role
alias
Name
Myositis Ossificans Progressiva
Role
alias
Name
Stone Man Syndrome
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Herb
HBDIS001067HBDIS002038
Me Sh
D009221
Omim
135100
Umls
C0016037C0027122
Icd10
M61.1
Med Dra
10068715
Sym Map
SMDE04805SMDE11261
Do Class
DOID:630DOID:7
Dis Ge Net
C0016037C0027122
Orphanet
337
Umls Sty
T047
Me Sh Class
C05
Etcm Disease
Fibrodysplasia Ossificans Progressiva
Tcmbank Disease
1187989
Itcmdb Generated
ITX-DISEASE-125C4ABF2C37ITX-DISEASE-96962E707692
Attributes
Merged source attributes and domain-specific metadata.
Version
v1,v2v2
Suppress
0
Page Title
Disease Fibrodysplasia Ossificans Progressiva Details page
Do Class Name
genetic disease; disease of anatomical entity
Disease Type
disease
Do Disease Class
disease of anatomical entity; genetic disease
Umls Disease Type
Disease or Syndrome
Basic Information
Disease Name
Fibrodysplasia Ossificans Progressiva
Global Category
Fetal diseases;Genetic diseases;Infectious diseases;Rare diseases
Anatomical Category
Bone diseases;Muscle diseases;Respiratory diseases;Skin diseases
Disease Definition
Fibrodysplasia ossificans progressiva (FOP) is a severely disabling heritable disorder of connective tissue characterized by congenital malformations of the great toes and progressive heterotopic ossiNCI2016_02D:A disorder characterized by non-neoplastic bone formation in soft tissues. It usually follows blunt trauma and bleeding in the deep soft tissues.|MSH2017_2016_08_12:A disease characterized by bony deposits or the ossification of muscle tissue.
Me Sh Disease Class
Musculoskeletal Diseases
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Musculoskeletal Diseases
Umls Semantic Type Name
Disease or Syndrome