Cardiomegaly

Symptom Information:

Symptom ID: HPO:0001640
Synonyms:
Cardiomegaly (disorder) [Orphanet:34200]
Cardiomegaly [Orphanet:34200]
Cardiomegaly [OMIM:Cardiomegaly]
Cardiomegaly [MedDRA:10007632]
Cardiac dilatation [MedDRA:10007632]
Cardiomegaly (excl hypertensive) [MedDRA:10007632]
Cardiomegaly NOS [MedDRA:10007632]
Enlargement heart [MedDRA:10007632]
Heart enlarged [MedDRA:10007632]
Megalocardia [MedDRA:10007632]
Cardiomegaly (rare) [OMIM:Cardiomegaly (rare)]
Cardiomegaly (type II, infantile) [OMIM:Cardiomegaly (type II, infantile)]
Quality:
Cross references:
Orphanet:34200 "Cardiomegaly" [Orphanet:34200]
OMIM: "Cardiomegaly" [OMIM:Cardiomegaly]
OMIM: "Cardiomegaly (rare)" [OMIM:Cardiomegaly (rare)]
OMIM: "Cardiomegaly (type II, infantile)" [OMIM:Cardiomegaly (type II, infantile)]
UMLS:C0018800 "Cardiomegaly" [HPO:0001640]
UMLS:C0018800 "Cardiomegaly" [Orphanet:34200]
Is a (Direct Parents):
HPO         Abnormal heart morphology
MedDRA Myocardial disorders NEC
Orphanet Structural anomalies of the cardio-circulatory system
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)
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)