DiseaseID 3664
上唇裂
disease
NCI2016_CDISC_1602D:Fissure or split of the upper lip. (Makris S, Solomon HM, Clark R, Shiota K, Barbellion S, Buschmann J, Ema M, Fujiwara M, Grote K, Hazelden KP, Hew KW, Horimoto M, Ooshima Y, Parkinson M, Wise LD. Te
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Disease: 1Experiment: 1Symptom: 12Target: 12Links: 25
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Record Fields
Scalar fields from the final disease record.
- Disease Id
- 3664
- Core Entity Id
- 59896
- Source Entity Count
- 1
- Preferred Name
- Cleft Upper Lip
- Name Cn
- 上唇裂
- Name Pinyin
- Shang Chun Lie
- Name En
- Cleft Upper Lip
- Name Latin
- Bilingual Status
- complete
- Disease Type
- disease
- Umls Disease Type
- Congenital Abnormality
- Disgenet Type
- disease
- Mesh Class
- Stomatognathic Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
- Do Class
- disease of anatomical entity; physical disorder; syndrome
- Hpo Class
- Abnormality of head or neck
- Mesh Class Name
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
- Hpo Class Name
- Abnormality of head or neck
- Do Class Name
- disease of anatomical entity; syndrome; physical disorder
- Disease Definition
- NCI2016_CDISC_1602D:Fissure or split of the upper lip. (Makris S, Solomon HM, Clark R, Shiota K, Barbellion S, Buschmann J, Ema M, Fujiwara M, Grote K, Hazelden KP, Hew KW, Horimoto M, Ooshima Y, Parkinson M, Wise LD. Terminology of developmental abnormalities in common laboratory mammals (Version 2). Part B. Birth Defects Res B Dev Reprod Toxicol. 2009 Aug;86(4):227-327.)|NCI2016_02D:A congenital abnormality consisting of one or more clefts (splits) in the upper lip, which may be accompanied by a cleft palate; it is the result of the failure of the embryonic parts of the lip to fuse.|MSH2017_2016_08_12:Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused by faulty migration of the mesoderm in the head region.|HPO2016_07_04:A gap in the upper lip. This is a congenital defect resulting from nonfusion of tissues of the lip during embryonal development. [HPO:probinson]|CSP2006:congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences; thought to be caused by faulty migration of the mesoderm in the head region.
- Version
- v2
- Suppressed
- No
Names
Preferred names, aliases, and source labels retained in the final schema.
Name
Cleft Upper Lip
Role
preferred
Name
Cleft Lip
Role
preferred
Name
Cleft Lip, Unilateral, Complete
Role
preferred
Name
Unilateral Cleft Lip
Role
preferred
Name
Cheiloschisis of Upper Lip
Role
alias
Name
Cleft Lip, Unilateral
Role
alias
Name
Cleft of Upper Lip
Role
alias
Name
Harelip
Role
alias
Name
One Sided Cleft Upper Lip
Role
alias
Name
Unilateral Cheiloschisis
Role
alias
Name
Unilateral Cleft Upper Lip
Role
alias
Cross References
Trusted external identifiers retained for this final record.
Hpo
HP:0000204HP:0100333
Herb
HBDIS000594HBDIS004068HBDIS008596
Me Sh
D002971
Umls
C0008924
Icd10
Q36Q36.9
Sym Map
SMDE07252
Do Class
DOID:0080015DOID:225DOID:7
Dis Ge Net
C0008924C0158651C0392006
Umls Sty
T019
Hpo Class
HP:0000152
Me Sh Class
C07C16
Tcmbank Disease
1058353968404
Attributes
Merged source attributes and domain-specific metadata.
Version
v2
Suppress
0
Do Class Name
disease of anatomical entity; syndrome; physical disorder
Disease Type
disease
Hpo Class Name
Abnormality of head or neck
Do Disease Class
disease of anatomical entity; physical disorder; syndrome
Hpo Disease Class
Abnormality of head or neck
Umls Disease Type
Congenital Abnormality
Disease Definition
NCI2016_CDISC_1602D:Fissure or split of the upper lip. (Makris S, Solomon HM, Clark R, Shiota K, Barbellion S, Buschmann J, Ema M, Fujiwara M, Grote K, Hazelden KP, Hew KW, Horimoto M, Ooshima Y, Parkinson M, Wise LD. Terminology of developmental abnormalities in common laboratory mammals (Version 2). Part B. Birth Defects Res B Dev Reprod Toxicol. 2009 Aug;86(4):227-327.)|NCI2016_02D:A congenital abnormality consisting of one or more clefts (splits) in the upper lip, which may be accompanied by a cleft palate; it is the result of the failure of the embryonic parts of the lip to fuse.|MSH2017_2016_08_12:Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused by faulty migration of the mesoderm in the head region.|HPO2016_07_04:A gap in the upper lip. This is a congenital defect resulting from nonfusion of tissues of the lip during embryonal development. [HPO:probinson]|CSP2006:congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences; thought to be caused by faulty migration of the mesoderm in the head region.
Me Sh Disease Class
Stomatognathic Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Stomatognathic Diseases
Umls Semantic Type Name
Congenital Abnormality