DiseaseID 7290

Uhl畸形

disease

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Disease: 1Experiment: 1Formula: 17Herb: 12Symptom: 4Target: 24Links: 58

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Record Fields

Scalar fields from the final disease record.

Disease Id: 7290
Core Entity Id: 64064
Source Entity Count: 1
Preferred Name: Uhl Anomaly
Name Cn: Uhl畸形
Name Pinyin: Uhl Ji Xing
Name En: Uhl Anomaly
Name Latin
Bilingual Status: complete
Disease Type: disease
Umls Disease Type: Congenital Abnormality
Disgenet Type: disease
Mesh Class: Cardiovascular DiseasesCardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Do Class: disease of anatomical entitydisease of anatomical entity; genetic disease
Hpo Class: Abnormality of the cardiovascular system
Mesh Class Name: Cardiovascular DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
Hpo Class Name: Abnormality of the cardiovascular system
Do Class Name: disease of anatomical entitygenetic disease; disease of anatomical entity
Disease Definition: NCI2016_02D:A rare genetic disorder characterized by cardiomyopathy affecting the right ventricle. The heart tissue is replaced by fibrous and adipose tissues. It is characterized by ventricular arrhythmia and right ventricular dysfunction. It is a cause of sudden death.|MSH2017_2016_08_12:A congenital cardiomyopathy that is characterized by infiltration of adipose and fibrous tissue into the RIGHT VENTRICLE wall and loss of myocardial cells. Primary injuries usually are at the free wall of right ventricular and right atria resulting in ventricular and supraventricular arrhythmias.
Version: v1
Suppressed: No

Names

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

Name

Uhl Anomaly

Role

preferred

Name

Arrhythmogenic Right Ventricular Dysplasia

Role

preferred

Name

Arrhythmogenic Right Ventricular Dysplasia, Familial, 1

Role

preferred

Name

Arrhythmogenic Right Ventricular Dysplasia, Familial, 10

Role

preferred

Name

Arrhythmogenic Right Ventricular Dysplasia, Familial, 11

Role

preferred

Name

Arrhythmogenic Right Ventricular Dysplasia, Familial, 12

Role

preferred

Name

Arrhythmogenic Right Ventricular Dysplasia, Familial, 2

Role

preferred

Name

Arrhythmogenic Right Ventricular Dysplasia, Familial, 8

Role

preferred

Name

Arrhythmogenic Right Ventricular Dysplasia, Familial, 9

Role

preferred

Name

ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1 (disorder)

Role

preferred

Name

ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 5 (disorder)

Role

preferred

Name

Other Cardiomyopathies

Role

preferred

Name

ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 1

Role

alias

Name

ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 10

Role

alias

Name

ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 11

Role

alias

Name

ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 12

Role

alias

Name

ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 2

Role

alias

Name

ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 8

Role

alias

Name

ARRHYTHMOGENIC RIGHT VENTRICULAR CARDIOMYOPATHY 9

Role

alias

Name

ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 11, AND MILD PALMOPLANTAR KERATODERMA WITH OR WITHOUT WOOLLY HAIR

Role

alias

Name

ARVC1

Role

alias

Name

ARVC10

Role

alias

Name

ARVC11

Role

alias

Name

ARVC12

Role

alias

Name

ARVC2

Role

alias

Name

ARVC8

Role

alias

Name

ARVC9

Role

alias

Name

ARVD1

Role

alias

Name

ARVD10

Role

alias

Name

ARVD11

Role

alias

Name

ARVD12

Role

alias

Name

ARVD2

Role

alias

Name

ARVD8

Role

alias

Name

ARVD9

Role

alias

Name

Arrhythmogenic Right Ventricular Cardiomyopathy

Role

alias

Name

Arrhythmogenic Right Ventricular Dysplasia 1

Role

alias

Name

Arrhythmogenic Right Ventricular Dysplasia 10

Role

alias

Name

Arrhythmogenic Right Ventricular Dysplasia 11

Role

alias

Name

Arrhythmogenic Right Ventricular Dysplasia 12

Role

alias

Name

Arrhythmogenic Right Ventricular Dysplasia 13

Role

alias

Name

Arrhythmogenic Right Ventricular Dysplasia 2

Role

alias

Name

Arrhythmogenic Right Ventricular Dysplasia 3

Role

alias

Name

Arrhythmogenic Right Ventricular Dysplasia 4

Role

alias

Name

Arrhythmogenic Right Ventricular Dysplasia 5

Role

alias

Name

Arrhythmogenic Right Ventricular Dysplasia 6

Role

alias

Name

Arrhythmogenic Right Ventricular Dysplasia 8

Role

alias

Name

Arrhythmogenic Right Ventricular Dysplasia 9

Role

alias

Name

Arrhythmogenic Right Ventricular Dysplasia, Familial, 5

Role

alias

Name

CARDIOMYOPATHY, RIGHT VENTRICULAR DILATED

Role

alias

Name

Uhl'S Anomaly

Role

alias

Cross References

Trusted external identifiers retained for this final record.

Hpo

HP:0011724

Herb

HBDIS005890HBDIS008437HBDIS008523HBDIS015128HBDIS015505HBDIS016069HBDIS017474HBDIS017533HBDIS017974HBDIS018136HBDIS018728

Me Sh

D019571

Omim

107970600996604400607450609040610193610476611528

Umls

C0265857C0349788C1832931C1836906C1843896C1857777C1862511C1862512C1864850C1969081C4310824

Icd10

I42.8

Sym Map

SMDE02227SMDE03177SMDE03300SMDE03353SMDE04503SMDE04907SMDE05037SMDE06028

Do Class

DOID:630DOID:7

Dis Ge Net

C0265857C0348617C0349788C1832931C1836906C1843896C1857777C1858379C1862511C1864850C1969081

Umls Sty

T019T047

Hpo Class

HP:0001626

Me Sh Class

C14C16

Etcm Disease

Arrhythmogenic Right Ventricular Dysplasia, Familial, 1Arrhythmogenic Right Ventricular Dysplasia, Familial, 10Arrhythmogenic Right Ventricular Dysplasia, Familial, 11Arrhythmogenic Right Ventricular Dysplasia, Familial, 12Arrhythmogenic Right Ventricular Dysplasia, Familial, 2Arrhythmogenic Right Ventricular Dysplasia, Familial, 8Arrhythmogenic Right Ventricular Dysplasia, Familial, 9

Tcmbank Disease

1291114521168862074822127271332903830550324767379390

Itcmdb Generated

ITX-DISEASE-45A4406E029CITX-DISEASE-4AAA4C505339ITX-DISEASE-70EFC57CC7F8ITX-DISEASE-92CB30CB39BBITX-DISEASE-9D7B092B49C6ITX-DISEASE-A5F284AE3AB6ITX-DISEASE-B63D857961C4ITX-DISEASE-CFF7D11AB96D

Attributes

Merged source attributes and domain-specific metadata.

Version

v1v1,v2v2

Suppress

Page Title

Disease Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 Details pageDisease Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 Details pageDisease Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 Details pageDisease Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 Details pageDisease Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 Details pageDisease Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 Details pageDisease Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 Details page

Do Class Name

disease of anatomical entitygenetic disease; disease of anatomical entity

Disease Type

disease

Hpo Class Name

Abnormality of the cardiovascular system

Do Disease Class

disease of anatomical entitydisease of anatomical entity; genetic disease

Hpo Disease Class

Abnormality of the cardiovascular system

Umls Disease Type

Congenital AbnormalityDisease or SyndromeDisease or Syndrome; Congenital Abnormality

Basic Information

Disease Name

Arrhythmogenic Right Ventricular Dysplasia, Familial, 1

Global Category

Genetic diseases;Rare diseases

Anatomical Category