Cardiomegaly
Symptom Information:
Symptom ID: | HPO:0001640 | ||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the cardiovascular system(HPO:0001626) Abnormal heart morphology(HPO:0001627) Cardiomegaly(HPO:0001640) MedDRA: Cardiac disorders(MedDRA:10007541) Abnormality of the myocardium(HPO:0001637) Myocardial disorders NEC(MedDRA:10028590) Cardiomegaly(HPO:0001640) |
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Database Frequency: | 81 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Alpha-N-acetylgalactosaminidase deficiency | (Orphanet:3137) |
Alpha-N-acetylgalactosaminidase deficiency type 2 | (Orphanet:79280) |
Alström syndrome | (Orphanet:64) |
Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
Beckwith-Wiedemann syndrome | (Orphanet:116) |
Beckwith-Wiedemann syndrome due to 11p15 microdeletion | (Orphanet:231127) |
Brachydactyly-long thumb syndrome | (Orphanet:2946) |
Cardiomyopathy, dilated, 1DD | (OMIM:613172) |
Cardiomyopathy, dilated, 1I | (OMIM:604765) |
Cardiomyopathy, dilated, 1M | (OMIM:607482) |
Cardiomyopathy, familial restrictive, 1 | (OMIM:115210) |
Carnitine palmitoyl transferase 1A deficiency | (Orphanet:156) |
Carnitine palmitoyl transferase II deficiency, neonatal form | (Orphanet:228308) |
Carnitine palmitoyl transferase II deficiency, severe infantile form | (Orphanet:228305) |
Carnitine uptake deficiency | (Orphanet:158) |
Cirrhotic cardiomyopathy | (Orphanet:57777) |
Combined oxidative phosphorylation defect type 8 | (Orphanet:319504) |
Congenital toxoplasmosis | (Orphanet:858) |
Craniofaciofrontodigital syndrome | (Orphanet:363705) |
ETHANOLAMINOSIS | (OMIM:227150) |
Ectodermal dysplasia - cutaneous syndactyly syndrome | (Orphanet:247827) |
Faisalabad histiocytosis | (Orphanet:254707) |
Familial amyloid polyneuropathy | (Orphanet:85447) |
Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease | (Orphanet:439854) |
Fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency | (Orphanet:289527) |
Fetal Gaucher disease | (Orphanet:85212) |
Free sialic acid storage disease, infantile form | (Orphanet:309324) |
Fucosidosis | (Orphanet:349) |
Gaucher disease - ophthalmoplegia - cardiovascular calcification | (Orphanet:2072) |
Glycogen storage disease due to LAMP-2 deficiency | (Orphanet:34587) |
Glycogen storage disease due to acid maltase deficiency | (Orphanet:365) |
Glycogen storage disease due to acid maltase deficiency, infantile onset | (Orphanet:308552) |
Glycogen storage disease due to glycogen debranching enzyme deficiency | (Orphanet:366) |
Greenberg dysplasia | (Orphanet:1426) |
H syndrome | (Orphanet:168569) |
Hemochromatosis, type 1 | (OMIM:235200) |
His bundle tachycardia | (Orphanet:3283) |
Histiocytoid cardiomyopathy | (Orphanet:137675) |
Hurler syndrome | (Orphanet:93473) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hypertrichotic osteochondrodysplasia, Cantu type | (Orphanet:1517) |
Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation | (Orphanet:324525) |
Isobutyryl-CoA dehydrogenase deficiency | (Orphanet:79159) |
Larsen-like syndrome, B3GAT3 type | (Orphanet:284139) |
Left ventricular noncompaction 10 | (OMIM:615396) |
Leprechaunism | (Orphanet:508) |
Lymphoid interstitial pneumonia | (Orphanet:79128) |
Microcephaly-cardiomyopathy syndrome | (Orphanet:2515) |
Mucolipidosis type 2 | (Orphanet:576) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mulibrey nanism | (Orphanet:2576) |
Multifocal atrial tachycardia | (Orphanet:3282) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Naxos disease | (Orphanet:34217) |
Neonatal hemochromatosis | (Orphanet:446) |
Nephronophthisis 9 | (OMIM:613824) |
Non-specific interstitial pneumonia | (Orphanet:91364) |
Pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome | (Orphanet:254723) |
Primary hyperoxaluria type 1 | (Orphanet:93598) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
Pulmonary capillary hemangiomatosis | (Orphanet:199241) |
Pulmonary venoocclusive disease | (Orphanet:31837) |
REFSUM DISEASE, CLASSIC | (OMIM:266500) |
Refsum disease | (Orphanet:773) |
Rosaï-Dorfman disease | (Orphanet:158014) |
SPONDYLOMETAPHYSEAL DYSPLASIA, MEGARBANE-DAGHER-MELKI TYPE | (OMIM:613320) |
Sandhoff disease | (Orphanet:796) |
Sandhoff disease, adult form | (Orphanet:309169) |
Sandhoff disease, infantile form | (Orphanet:309155) |
Sandhoff disease, juvenile form | (Orphanet:309162) |
Sanfilippo syndrome type B | (Orphanet:79270) |
Sialidosis type 1 | (Orphanet:812) |
Sickle cell anemia | (Orphanet:232) |
Singleton-Merten dysplasia | (Orphanet:85191) |
Timothy syndrome | (Orphanet:65283) |
Very long chain acyl-CoA dehydrogenase deficiency | (Orphanet:26793) |
Williams syndrome | (Orphanet:904) |
Wolcott-Rallison syndrome | (Orphanet:1667) |
X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome | (Orphanet:324410) |
[DEL] GLYCOGEN STORAGE DISEASE OF HEART, LETHAL CONGENITAL | (OMIM:261740) |