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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine



   criss-cross heart
  

Disease ID 1698
Disease criss-cross heart
Definition
A developmental malformation of the heart characterized by a twisted but not defective atrioventicular connection. The abnormal rotation of the ventricular mass around its long axis results in the crossing of the inflow streams of the two ventricles. Other features include hypoplasia of the TRICUSPID VALVE and RIGHT VENTRICLE.
Synonym
criss cross heart
criss-cross heart (disorder)
criss-cross hearts
crisscross heart
crisscross heart [disease/finding]
crisscross hearts
heart, criss-cross
heart, crisscross
hearts, criss-cross
hearts, crisscross
twisted atrioventricular connections
Orphanet
UMLS
C0010334
MeSH
SNOMED-CT
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:1)
Curated Gene(Waiting for update.)
Inferring Gene(Waiting for update.)
Text Mined Gene(Waiting for update.)
Locus(Waiting for update.)
Disease ID 1698
Disease criss-cross heart
Integrated Phenotype
HPO | Name(Total Integrated Phenotypes:13)
HP:0000961  |  Cyanosis
HP:0001633  |  Abnormality of the mitral valve
HP:0002093  |  Respiratory insufficiency
HP:0002564  |  Malformation of the heart and great vessels
HP:0001629  |  Ventricular septal defect
HP:0001669  |  Transposition of the great arteries
HP:0010446  |  Tricuspid stenosis
HP:0000765  |  Abnormality of the thorax
HP:0001999  |  Abnormal facial shape
HP:0004381  |  Supravalvular aortic stenosis
HP:0001718  |  Mitral stenosis
HP:0001642  |  Pulmonic stenosis
HP:0011968  |  Feeding difficulties
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:3)
Disease ID 1698
Disease criss-cross heart
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
Text Mining Genotype(Total Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:0)
(Waiting for update.)
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:8)
HP ID HP Name MP ID MP Name Annotation
HP:0001999Abnormal facial shapeMP:0008018increased facial tumor incidencegreater than the expected number of neoplasms on the face, usually in the form of a distinct mass, in a specific population in a given time period
HP:0001642Pulmonic stenosisMP:0010449heart right ventricle outflow tract stenosisabnormal constriction or narrowing of part of the anteriosuperior, smooth-walled portion of the cavity of the right ventricle, beginning at the supraventricular crest and terminating in the pulmonary trunk
HP:0000765Abnormality of the thoraxMP:0013620increased internal diameter of femurincreased cross-sectional distance that extends from one lateral edge of the femur long bone marrow cavity, through its center and to the opposite lateral edge of the bone marrow cavity through the mid point of the femur
HP:0001718Mitral stenosisMP:0006117aortic valve stenosisabnormal narrowing of the aortic valve
HP:0001629Ventricular septal defectMP:0011667double outlet right ventricle with atrioventricular septal defecta form of DORV in which there is also a complete atrioventricular canal
HP:0001633Abnormality of the mitral valveMP:0010919increased number of pulmonary neuroendocrine bodiesgreater number of the corpuscular, organoid structures composed of PNECs, found as distinctive innervated clusters only within intrapulmonary airways, where they appear concentrated at airway branch points; NEBs reach from the basement membrane to the air
HP:0004381Supravalvular aortic stenosisMP:0010641descending aorta stenosisdiffuse constriction or narrowing of the descending aorta
HP:0001669Transposition of the great arteriesMP:0012129failure of blastocyst formationinability to form a blastocyst from a solid ball of cells known as a morula
Mapped by homologous gene(Total Items:12)
HP ID HP Name MP ID MP Name Annotation
HP:0002093Respiratory insufficiencyMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0010446Tricuspid stenosisMP:0011108embryonic lethality during organogenesis, incomplete penetrancethe appearance of lower than Mendelian ratios of organisms of a given genotype due to death of some, but not all of the organisms between embryo turning and the completion of organogenesis (Mus: E9-9.5 to less than E14)
HP:0001629Ventricular septal defectMP:3000003abnormal Ebner's gland morphologyany structural anomaly of the serous salivary glands which reside adjacent to the moats surrounding the circumvallate and foliate papillae just anterior to the posterior third of the tongue, anterior to the terminal sulcus; these exocrine glands secrete l
HP:0011968Feeding difficultiesMP:0020234decreased basal metabolismdecrease in heat production of an organism at the lowest level of cell chemistry in an inactive, awake, and fasting state
HP:0004381Supravalvular aortic stenosisMP:0020321increased vascular endothelial cell apoptosisincrease in the timing or the number of vascular endothelial cells undergoing programmed cell death
HP:0001642Pulmonic stenosisMP:0020040decreased bone ossificationdecrease in the formation of bone or of a bony substance, or the conversion of fibrous tissue or of cartilage into bone or a bony substance
HP:0001669Transposition of the great arteriesMP:0013901absent female preputial glandabsence of the paired, lobulated, modified sebaceous glands located on the side of the clitoris in female rodents; in contrast to the preputial glands in male rodents, clitoral glands are a minor source of olfactory stimuli contributing to sexual attracti
HP:0001718Mitral stenosisMP:0020039increased bone ossificationincrease in the formation of bone or of a bony substance, or the conversion of fibrous tissue or of cartilage into bone or a bony substance
HP:0001633Abnormality of the mitral valveMP:0014164abnormal ciliary process morphology any structural anomaly of any of the pigmented processes that radiate from the ciliary muscle and give attachments to ligaments supporting the lens of the eye; these processes increase in thickness as they advance from the orbiculus ciliaris to the exter
HP:0000765Abnormality of the thoraxMP:0020254decreased collagen leveldecreased level of the main structural protein of the various connective tissues in animals
HP:0000961CyanosisMP:0013781abnormal mammary gland luminal epithelium morphologyany structural anomaly of the inner cell layer of the mammary epithelium bilayer that lines the luminal surface of mammary gland ducts and alveoli; luminal cells have only limited contact with the underlying basement membrane and surrounding connective ti
HP:0001999Abnormal facial shapeMP:0020309increased creatine kinase activityincreased ability of to catalyze the reaction: ATP + creatine = N-phosphocreatine + ADP + 2 H(+).
Disease ID 1698
Disease criss-cross heart
Case(Waiting for update.)