ITCMDBv1
DiseaseID 14568

多脾症

disease

NCI2016_CDISC_1602D:Mirror-image transposition of the abdominal and/or thoracic viscera. (Makris S, Solomon HM, Clark R, Shiota K, Barbellion S, Buschmann J, Ema M, Fujiwara M, Grote K, Hazelden KP, Hew KW, Horimoto M, O

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Relationship Network

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

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Disease: 1Formula: 11Herb: 12Symptom: 4Target: 24Links: 51
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Record Fields

Scalar fields from the final disease record.

Disease Id
14568
Core Entity Id
72373
Source Entity Count
1
Preferred Name
Polyasplenia
Name Cn
多脾症
Name Pinyin
Duo Pi Zheng
Name En
Polyasplenia
Name Latin
Bilingual Status
complete
Disease Type
disease
Umls Disease Type
Congenital Abnormality
Disgenet Type
disease
Mesh Class
Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesCardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities
Do Class
genetic disease; physical disorderphysical disorder
Hpo Class
Abnormality of the cardiovascular systemGrowth abnormalityGrowth abnormality; Abnormality of the cardiovascular systemGrowth abnormality; Abnormality of the digestive system; Abnormality of the cardiovascular system
Mesh Class Name
Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases
Hpo Class Name
Abnormality of the cardiovascular systemAbnormality of the cardiovascular system; Growth abnormalityAbnormality of the digestive system; Abnormality of the cardiovascular system; Growth abnormalityGrowth abnormality
Do Class Name
genetic disease; physical disorderphysical disorder
Disease Definition
NCI2016_CDISC_1602D:Mirror-image transposition of the abdominal and/or thoracic viscera. (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 condition in which there is complete right-to-left reversal of the position of the major thoracic and abdominal organs (that is, they are arranged in a mirror image of the normal positioning).|MSH2017_2016_08_12:A congenital abnormality in which organs in the THORAX and the ABDOMEN are opposite to their normal positions (situs solitus) due to lateral transposition. Normally the STOMACH and SPLEEN are on the left, LIVER on the right, the three-lobed right lung is on the right, and the two-lobed left lung on the left. Situs inversus has a familial pattern and has been associated with a number of genes related to microtubule-associated proteins.|HPO2016_07_04:A left-right reversal (or mirror reflection") of the anatomical location of the viscera of the abdomen." [HPO:probinson]
Version
v1
Suppressed
No

Names

Preferred names, aliases, and source labels retained in the final schema.

Name
Polyasplenia
Role
preferred
Name
Heterotaxy, Visceral, 1, X-Linked
Role
preferred
Name
Heterotaxy, Visceral, 2, Autosomal
Role
preferred
Name
Heterotaxy, Visceral, 4, Autosomal
Role
preferred
Name
Heterotaxy, Visceral, 5, Autosomal
Role
preferred
Name
Heterotaxy, Visceral, 6, Autosomal
Role
preferred
Name
Right Atrial Isomerism
Role
preferred
Name
Situs Inversus
Role
preferred
Name
Asplenia Syndrome
Role
preferred
Name
CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED
Role
preferred
Name
Dextrocardia With Situs Inversus
Role
preferred
Name
Heterotaxy Syndrome
Role
preferred
Name
Heterotaxy, Visceral, 3, Autosomal
Role
preferred
Name
Heterotaxy, Visceroatrial, Autosomal Recessive
Role
preferred
Name
Isomerism of Atrial Appendages
Role
preferred
Name
Isomerism of Atrial Appendages With Asplenia Or Polysplenia
Role
preferred
Name
Left Atrial Isomerism
Role
preferred
Name
Polysplenia Syndrome
Role
preferred
Name
Situs Ambiguus
Role
preferred
Name
Situs Inversus Totalis
Role
preferred
Name
VAH, AUTOSOMAL RECESSIVE
Role
preferred
Name
ASPLENIA WITH CARDIOVASCULAR ANOMALIES
Role
alias
Name
Abdominal Situs Inversus
Role
alias
Name
Ambiguus, Situs
Role
alias
Name
CHTD1
Role
alias
Name
DEXTROCARDIA WITH OTHER CARDIAC MALFORMATIONS
Role
alias
Name
HTX
Role
alias
Name
HTX1
Role
alias
Name
HTX2
Role
alias
Name
HTX4
Role
alias
Name
HTX5
Role
alias
Name
HTX6
Role
alias
Name
Heterotaxia
Role
alias
Name
Heterotaxy
Role
alias
Name
Heterotaxy, Visceral, X-Linked
Role
alias
Name
IVEMARK SYNDROME
Role
alias
Name
LATERALITY, X-LINKED
Role
alias
Name
RAI
Role
alias
Name
Right Isomerism
Role
alias
Name
Right-Sided Isomerism
Role
alias
Name
SITUS INVERSUS VISCERUM
Role
alias
Name
SITUS INVERSUS, COMPLEX CARDIAC DEFECTS, AND SPLENIC DEFECTS, X-LINKED
Role
alias
Name
SIV
Role
alias
Name
Situs Inversus Visceralis
Role
alias
Name
Situs Oppositus
Role
alias
Name
Situs Transversus
Role
alias
Name
Visceral Heterotaxy
Role
alias

Cross References

Trusted external identifiers retained for this final record.

Hpo
HP:0001696HP:0003363HP:0011536HP:0011537HP:0030853HP:0031855
Herb
HBDIS002762HBDIS004187HBDIS005829HBDIS006040HBDIS008238HBDIS014214HBDIS016080HBDIS016955HBDIS018508HBDIS018509HBDIS018510HBDIS020104HBDIS020747HBDIS020854HBDIS020944HBDIS020945HBDIS020946HBDIS021506HBDIS021776HBDIS027198HBDIS028715
Me Sh
D012857D059446
Omim
208530306955605376606325613751614779
Umls
C0037221C0175707C0265357C1415817C1844020C1876171C1876172C1876173C3151057C3151867C3178806C3495537C3553676
Icd10
Q20.6Q89.3
Sym Map
SMDE00315SMDE00896SMDE01082SMDE01351SMDE02438SMDE02871SMDE13181
Do Class
DOID:0080015DOID:630
Dis Ge Net
C0037221C0175707C0265357C0266642C0344692C1395317C1415817C1844020C1853444C1876171C1876172C1876173C2910124C3151057C3151867C3178805C3178806C3178807C3495537C3553676C4551493
Umls Sty
T019T047
Hpo Class
HP:0001507HP:0001626HP:0025031
Me Sh Class
C14C15C16
Etcm Disease
Heterotaxy, Visceral, 1, X-LinkedHeterotaxy, Visceral, 2, AutosomalHeterotaxy, Visceral, 3, AutosomalHeterotaxy, Visceral, 4, AutosomalHeterotaxy, Visceral, 5, AutosomalHeterotaxy, Visceral, 6, Autosomal
Tcmbank Disease
13171134991374619138217982184424171257872586827023274442763428459306163162644365407771281779256
Itcmdb Generated
ITX-DISEASE-0E7364FB78BEITX-DISEASE-2F5F62B4A325ITX-DISEASE-53DC97124A2CITX-DISEASE-5720528F81C4ITX-DISEASE-8823E79B35A7ITX-DISEASE-8FF18692278EITX-DISEASE-B4589A805E0CITX-DISEASE-C7305375B583ITX-DISEASE-D09A8D984BCA

Attributes

Merged source attributes and domain-specific metadata.

Version
v1v2
Suppress
0
Page Title
Disease Heterotaxy, Visceral, 1, X-Linked Details pageDisease Heterotaxy, Visceral, 2, Autosomal Details pageDisease Heterotaxy, Visceral, 3, Autosomal Details pageDisease Heterotaxy, Visceral, 4, Autosomal Details pageDisease Heterotaxy, Visceral, 5, Autosomal Details pageDisease Heterotaxy, Visceral, 6, Autosomal Details page
Do Class Name
genetic disease; physical disorderphysical disorder
Disease Type
disease
Hpo Class Name
Abnormality of the cardiovascular systemAbnormality of the cardiovascular system; Growth abnormalityAbnormality of the digestive system; Abnormality of the cardiovascular system; Growth abnormalityGrowth abnormality
Do Disease Class
genetic disease; physical disorderphysical disorder
Hpo Disease Class
Abnormality of the cardiovascular systemGrowth abnormalityGrowth abnormality; Abnormality of the cardiovascular systemGrowth abnormality; Abnormality of the digestive system; Abnormality of the cardiovascular system
Umls Disease Type
Congenital AbnormalityDisease or Syndrome
Basic Information
Disease Name
Heterotaxy, Visceral, 1, X-Linked
Global Category
Genetic diseases;Rare diseases
Anatomical Category
Immune diseases
Disease Name
Heterotaxy, Visceral, 2, Autosomal
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Cardiovascular diseases
Disease Name
Heterotaxy, Visceral, 3, Autosomal
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Cardiovascular diseases
Disease Name
Heterotaxy, Visceral, 4, Autosomal
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Cardiovascular diseases
Disease Name
Heterotaxy, Visceral, 5, Autosomal
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Cardiovascular diseases
Disease Name
Heterotaxy, Visceral, 6, Autosomal
Global Category
Fetal diseases;Genetic diseases;Rare diseases
Anatomical Category
Cardiovascular diseases
Disease Definition
NCI2016_CDISC_1602D:Mirror-image transposition of the abdominal and/or thoracic viscera. (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 condition in which there is complete right-to-left reversal of the position of the major thoracic and abdominal organs (that is, they are arranged in a mirror image of the normal positioning).|MSH2017_2016_08_12:A congenital abnormality in which organs in the THORAX and the ABDOMEN are opposite to their normal positions (situs solitus) due to lateral transposition. Normally the STOMACH and SPLEEN are on the left, LIVER on the right, the three-lobed right lung is on the right, and the two-lobed left lung on the left. Situs inversus has a familial pattern and has been associated with a number of genes related to microtubule-associated proteins.|HPO2016_07_04:A left-right reversal (or mirror reflection") of the anatomical location of the viscera of the abdomen." [HPO:probinson]
Me Sh Disease Class
Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesCardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities
Dis Ge Net Disease Type
disease
Disease Class Name Me Sh
Congenital, Hereditary, and Neonatal Diseases and AbnormalitiesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases; Cardiovascular Diseases
Umls Semantic Type Name
Congenital AbnormalityDisease or Syndrome