DiseaseID 4016
扁平足
disease
MSH2017_2016_08_12:A foot anomaly in which one or more of the arches of the foot have flattened out.|HPO2016_07_04:A foot where the longitudinal arch of the foot is in contact with the ground or floor when the individual
Relationship Network
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Disease: 1Symptom: 1Target: 12Links: 13
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 4016
- Core Entity Id
- 60300
- Source Entity Count
- 1
- Preferred Name
- Flatfoot
- Name Cn
- 扁平足
- Name Pinyin
- Bian Ping Zu
- Name En
- Flatfoot
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Acquired Abnormality
- 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
- Hpo Class
- Abnormality of limbsAbnormality of the skeletal system; Abnormality of limbs
- 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
- Abnormality of limbsAbnormality of limbs; Abnormality of the skeletal system
- Do Class Name
- Disease Definition
- MSH2017_2016_08_12:A foot anomaly in which one or more of the arches of the foot have flattened out.|HPO2016_07_04:A foot where the longitudinal arch of the foot is in contact with the ground or floor when the individual is standing; or, in a patient lying supine, a foot where the arch is in contact with the surface of a flat board pressed against the sole of the foot by the examiner with a pressure similar to that expected from weight bearing; or, the height of the arch is reduced. [HPO:probinson, pmid:19125433]
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Flatfoot
Role
preferred
Name
Acquired Flat Foot
Role
preferred
Name
Talipes Calcaneovalgus
Role
preferred
Name
Vertical Talus
Role
preferred
Name
Congenital Vertical Talus
Role
alias
Name
Dropped Arches
Role
alias
Name
Fallen Arches
Role
alias
Name
Flat Feet
Role
alias
Name
Flat Foot
Role
alias
Name
Flat Foot [Pes Planus] (Acquired)
Role
alias
Name
Pes Calcaneovarus
Role
alias
Name
Pes Planus
Role
alias
Name
Rocker Bottom Feet
Role
alias
Name
Rocker Bottom Foot
Role
alias
Name
Rocker-Bottom Foot
Role
alias
Name
Vertical Talus, Congenital
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0001763HP:0001838HP:0001884
Herb
HBDIS001082HBDIS003703HBDIS005318HBDIS005643
Me Sh
D005413
Omim
192950
Umls
C0016202
Icd10
M21.4
Sym Map
SMDE08775
Dis Ge Net
C0016202C0152237C0240912C0264133
Umls Sty
T019T020T190
Hpo Class
HP:0000924HP:0040064
Me Sh Class
C05C16C17
Tcmbank Disease
165516762322825504652
Itcmdb Generated
ITX-DISEASE-002A8F0AEB15ITX-DISEASE-C37A0BF01D63
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Disease Type
diseasephenotype
Hpo Class Name
Abnormality of limbsAbnormality of limbs; Abnormality of the skeletal system
Hpo Disease Class
Abnormality of limbsAbnormality of the skeletal system; Abnormality of limbs
Umls Disease Type
Acquired AbnormalityAnatomical AbnormalityCongenital Abnormality
Disease Definition
MSH2017_2016_08_12:A foot anomaly in which one or more of the arches of the foot have flattened out.|HPO2016_07_04:A foot where the longitudinal arch of the foot is in contact with the ground or floor when the individual is standing; or, in a patient lying supine, a foot where the arch is in contact with the surface of a flat board pressed against the sole of the foot by the examiner with a pressure similar to that expected from weight bearing; or, the height of the arch is reduced. [HPO:probinson, pmid:19125433]
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
diseasephenotype
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
Acquired AbnormalityAnatomical AbnormalityCongenital Abnormality