DiseaseID 17201
裂足
disease
NCI2016_02D:Split-hand/foot malformation mapped to chromosome 10q24.
Relationship Network
Interactive first-hop connections across herbs, ingredients, formulas, targets, diseases, symptoms, syndromes, evidence, and monographs.
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Disease: 1Symptom: 1Target: 12Links: 13
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 17201
- Core Entity Id
- 75392
- Source Entity Count
- 1
- Preferred Name
- Split Foot
- Name Cn
- 裂足
- Name Pinyin
- Lie Zu
- Name En
- Split Foot
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal DiseasesStomatognathic Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
- Do Class
- disease of anatomical entitydisease of anatomical entity; genetic disease
- Hpo Class
- Abnormality 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; Musculoskeletal Diseases; Stomatognathic Diseases
- Hpo Class Name
- Abnormality of limbs; Abnormality of the skeletal system
- Do Class Name
- disease of anatomical entitygenetic disease; disease of anatomical entity
- Disease Definition
- NCI2016_02D:Split-hand/foot malformation mapped to chromosome 10q24.
- Version
- v1
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Split Foot
Role
preferred
Name
Split Hand-Split Foot Malformation
Role
preferred
Name
Split-Hand/Foot Malformation 3
Role
preferred
Name
Split-Hand/Foot Malformation 4
Role
preferred
Name
Ectrodactyly
Role
preferred
Name
SPLIT-HAND/FOOT MALFORMATION 6 (disorder)
Role
preferred
Name
Split Hand Foot Deformity 1
Role
preferred
Name
Split-Hand/Foot Malformation 2
Role
preferred
Name
Cleft Hand
Role
alias
Name
Foot Ectrodactyly
Role
alias
Name
Limb Deficiencies, Distal, With Micrognathia
Role
alias
Name
Lobster Claw Hand
Role
alias
Name
Lobster-Claw Foot Deformity
Role
alias
Name
Lobster-Claw Hand
Role
alias
Name
Lobster-claw Deformity
Role
alias
Name
SHFM
Role
alias
Name
SHFM4
Role
alias
Name
Shfm6
Role
alias
Name
Split Hand Foot Malformation
Role
alias
Name
Split Hand-Foot Malformation
Role
alias
Name
Split Hand-Foot Malformation 1
Role
alias
Name
Split Hand-Foot Malformation 2
Role
alias
Name
Split Hand-Foot Malformation 3
Role
alias
Name
Split Hand-Foot Malformation 4
Role
alias
Name
Split Hand-Foot Malformation 5
Role
alias
Name
Split Hand-Foot Malformation 6
Role
alias
Name
Split-Foot
Role
alias
Name
Split-Hand-Foot Malformation 4
Role
alias
Name
Split-Hand/Foot Deformity 1
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0001839HP:0100257
Herb
HBDIS005850HBDIS009374HBDIS015703HBDIS017036HBDIS019812HBDIS020198HBDIS028824
Omim
183600225300313350605289
Umls
C0265554C1838652C1854442
Icd10
Q71.6Q72.7
Sym Map
SMDE01500SMDE04870SMDE13375
Do Class
DOID:630DOID:7
Dis Ge Net
C0265554C0432028C1838652C1839258C1854442C2749665C2931019
Orphanet
2440
Umls Sty
T019T047
Hpo Class
HP:0000924HP:0040064
Me Sh Class
C05C07C16
Tcmbank Disease
12896166101899119800320416984
Attributes
Merged source attributes and domain-specific metadata.
Version
v1v1,v2v2
Suppress
0
Do Class Name
disease of anatomical entitygenetic disease; disease of anatomical entity
Disease Type
disease
Hpo Class Name
Abnormality of limbs; Abnormality of the skeletal system
Do Disease Class
disease of anatomical entitydisease of anatomical entity; genetic disease
Hpo Disease Class
Abnormality of the skeletal system; Abnormality of limbs
Umls Disease Type
Congenital AbnormalityDisease or Syndrome
Disease Definition
NCI2016_02D:Split-hand/foot malformation mapped to chromosome 10q24.Split hand-split foot malformation (SHFM) refers to a spectrum of genetically and clinically heterogenous terminal limb defect (see this term) characterized by hypoplasia/ absence of central rays of t
Me Sh Disease Class
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal DiseasesStomatognathic 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; Musculoskeletal Diseases; Stomatognathic Diseases
Umls Semantic Type Name
Congenital AbnormalityDisease or Syndrome