Congestive heart failure, and Myocardial infarction

Diseases related with Congestive heart failure and Myocardial infarction

In the following list you will find some of the most common rare diseases related to Congestive heart failure and Myocardial infarction that can help you solving undiagnosed cases.


Top matches:

High match CARDIOMYOPATHY, DILATED, 1V; CMD1V


Related symptoms:

  • Cardiomyopathy
  • Congestive heart failure
  • Dementia
  • Dilated cardiomyopathy
  • Syncope


SOURCES: OMIM MESH MENDELIAN

More info about CARDIOMYOPATHY, DILATED, 1V; CMD1V

High match CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11; CMH11


Related symptoms:

  • Cardiomyopathy
  • Atrial septal defect
  • Congestive heart failure
  • Arrhythmia
  • Dyspnea


SOURCES: OMIM MESH MENDELIAN

More info about CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11; CMH11

High match CARDIOMYOPATHY, DILATED, 1Y; CMD1Y


Related symptoms:

  • Pain
  • Respiratory distress
  • Cardiomyopathy
  • Edema
  • Atrial septal defect


SOURCES: OMIM MESH MENDELIAN

More info about CARDIOMYOPATHY, DILATED, 1Y; CMD1Y

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Other less relevant matches:

High match OBESITY DUE TO CEP19 DEFICIENCY


Related symptoms:

  • Intellectual disability
  • Hypertension
  • Congestive heart failure
  • Obesity
  • Diabetes mellitus


SOURCES: OMIM ORPHANET MENDELIAN

More info about OBESITY DUE TO CEP19 DEFICIENCY

High match GENERALIZED ARTERIAL CALCIFICATION OF INFANCY


Idiopathic arterial calcification of infancy is a rare condition characterized by extensive calcification and stenosis of the large and medium sized arteries.

GENERALIZED ARTERIAL CALCIFICATION OF INFANCY Is also known as idiopathic infantile arterial calcification|infantile arteriosclerosis|occlusive infantile arteriopathy|idiopathic obliterative arteriopathy

Related symptoms:

  • Hypertension
  • Congestive heart failure
  • Dilatation
  • Papule
  • Tachycardia


SOURCES: ORPHANET OMIM MENDELIAN

More info about GENERALIZED ARTERIAL CALCIFICATION OF INFANCY

High match CONGENITAL MUSCULAR DYSTROPHY DUE TO LMNA MUTATION


Congenital muscular dystrophy due to LMNA mutation is a rare congenital muscular dystrophy characterized by prominent axial hypotonia, dropped head syndrome, predominantly proximal muscle weakness in upper limbs/distal in lower limbs (with absent, poor or lost motor development), joint contractures (initially distal, later proximal), spine rigidity, and early respiratory insufficiency, in the presence of moderately elevated serum creatine kinase. Cardiac arrhythmias and sudden death have been also reported.

CONGENITAL MUSCULAR DYSTROPHY DUE TO LMNA MUTATION Is also known as mdcl|lmna-related congenital muscular dystrophy|l-cmd

Related symptoms:

  • Global developmental delay
  • Generalized hypotonia
  • Growth delay
  • Failure to thrive
  • Muscle weakness


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about CONGENITAL MUSCULAR DYSTROPHY DUE TO LMNA MUTATION

High match ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1


Generalized arterial calcification of infancy (GACI) is a severe autosomal recessive disorder characterized by calcification of the internal elastic lamina of muscular arteries and stenosis due to myointimal proliferation. GACI is often fatal within the first 6 months of life because of myocardial ischemia resulting in refractory heart failure (summary by Rutsch et al., 2003 and Cheng et al., 2005). Genetic Heterogeneity of Arterial CalcificationGeneralized arterial calcification of infancy-2 (GACI2 ) is caused by mutation in the ABCC6 gene (OMIM ) on chromosome 16p13.Homozygous or compound heterozygous mutation in the NT5E gene (OMIM ) can cause adult-onset of calcification of arteries and joints (OMIM ).

ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1 Is also known as iiac|idiopathic infantile arterial calcification|gaci|arteriopathy, occlusive infantile|arterial calcification, idiopathic infantile

Related symptoms:

  • Short stature
  • Hearing impairment
  • Failure to thrive
  • Hypertension
  • Respiratory distress


SOURCES: OMIM MENDELIAN

More info about ARTERIAL CALCIFICATION, GENERALIZED, OF INFANCY, 1; GACI1

High match PPARG-RELATED FAMILIAL PARTIAL LIPODYSTROPHY


This type can be caused by mutation in the gene encoding PEROXISOME PROLIFERATOR-ACTIVATED RECEPTOR GAMMA.

PPARG-RELATED FAMILIAL PARTIAL LIPODYSTROPHY Is also known as familial partial lipodystrophy type 3|fpld3|pparg-related fpld|lipodystrophy, familial partial, associated with pparg mutations

Related symptoms:

  • Hypertension
  • Hepatomegaly
  • Myopathy
  • Congestive heart failure
  • Splenomegaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about PPARG-RELATED FAMILIAL PARTIAL LIPODYSTROPHY

High match MYOPATHY, MYOFIBRILLAR, 1; MFM1


Myofibrillar myopathy (MFM) is a noncommittal term that refers to a group of morphologically homogeneous, but genetically heterogeneous chronic neuromuscular disorders. The morphologic changes in skeletal muscle in MFM result from disintegration of the sarcomeric Z disc and the myofibrils, followed by abnormal ectopic accumulation of multiple proteins involved in the structure of the Z disc, including desmin, alpha-B-crystallin (CRYAB ), dystrophin (OMIM ), and myotilin (TTID ). Genetic Heterogeneity of Myofibrillar MyopathyOther forms of MFM include MFM2 (OMIM ), caused by mutation in the CRYAB gene (OMIM ); MFM3 (OMIM ) (OMIM ), caused by mutation in the MYOT gene (OMIM ); MFM4 (OMIM ), caused by mutation in the ZASP gene (LDB3 ); MFM5 (OMIM ), caused by mutation in the FLNC gene (OMIM ); MFM6 (OMIM ), caused by mutation in the BAG3 gene (OMIM ); MFM7 (OMIM ), caused by mutation in the KY gene (OMIM ); and MFM8 (OMIM ), caused by mutation in the PYROXD1 gene (OMIM ).'Desmin-related myopathy' is another term referring to MFM in which there are intrasarcoplasmic aggregates of desmin, usually in addition to other sarcomeric proteins. Rigid spine syndrome (OMIM ), caused by mutation in the SEPN1 gene (OMIM ), is another desmin-related myopathy. Goebel (1995) provided a review of desmin-related myopathy.

MYOPATHY, MYOFIBRILLAR, 1; MFM1 Is also known as drm|cardiomyopathy, dilated, with conduction defect and muscular dystrophy|cardiomyopathy, dilated, 1f and limb-girdle muscular dystrophy type 1d, formerly|myopathy, myofibrillar, desmin-related|lgmd2r, formerly|desminopathy, primary|arvd7, formerly|cmd1f

Related symptoms:

  • Scoliosis
  • Muscle weakness
  • Pain
  • Cataract
  • Flexion contracture


SOURCES: ORPHANET OMIM MENDELIAN

More info about MYOPATHY, MYOFIBRILLAR, 1; MFM1

High match AUTOSOMAL DOMINANT EMERY-DREIFUSS MUSCULAR DYSTROPHY


EDMD is characterized by myopathic changes in certain skeletal muscles and early contractures at the neck, elbows, and Achilles tendons, as well as cardiac conduction defects. 'Classic' Emery-Dreifuss muscular dystrophy (EDMD1 ) is an X-linked disorder caused by mutation in the emerin gene (EMD ) on Xq28 (Emery, 1989).For a discussion of genetic heterogeneity of EDMD, see {310300}.

AUTOSOMAL DOMINANT EMERY-DREIFUSS MUSCULAR DYSTROPHY Is also known as scapuloilioperoneal atrophy with cardiopathy|emd2|muscular dystrophy, limb-girdle, type 1b, formerly|emery-dreifuss muscular dystrophy, autosomal dominant|edmd2|cardiomyopathy, dilated, with quadriceps myopathy|muscular dystrophy, proximal, type 1b, forme

Related symptoms:

  • Intellectual disability
  • Generalized hypotonia
  • Scoliosis
  • Muscle weakness
  • Muscular hypotonia


SOURCES: OMIM ORPHANET MENDELIAN

More info about AUTOSOMAL DOMINANT EMERY-DREIFUSS MUSCULAR DYSTROPHY

Top 5 symptoms//phenotypes associated to Congestive heart failure and Myocardial infarction

Symptoms // Phenotype % cases
Cardiomyopathy Uncommon - Between 30% and 50% cases
Dilated cardiomyopathy Uncommon - Between 30% and 50% cases
Hypertrophic cardiomyopathy Uncommon - Between 30% and 50% cases
Dyspnea Uncommon - Between 30% and 50% cases
Hypertension Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Congestive heart failure and Myocardial infarction. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Atrial fibrillation Sudden cardiac death Arrhythmia Myopathy Respiratory insufficiency Tachycardia Elevated serum creatine phosphokinase Muscular dystrophy Gait disturbance Respiratory insufficiency due to muscle weakness Flexion contracture Muscle weakness Hypertriglyceridemia Spinal rigidity Palpitations Limb muscle weakness Respiratory distress Heart block Syncope Ventricular hypertrophy

Rare Symptoms - Less than 30% cases


Muscular hypotonia Mitral regurgitation Feeding difficulties Skeletal muscle atrophy Myalgia Atrial septal defect Left ventricular hypertrophy Hyperlordosis Bundle branch block Failure to thrive Neck muscle weakness Limb-girdle muscle weakness Pneumonia Rimmed vacuoles Progressive proximal muscle weakness Elbow flexion contracture Proximal muscle weakness Facial palsy Joint stiffness Lower limb muscle weakness Vertigo Progressive muscle weakness Scapular winging Generalized arterial calcification EMG: myopathic abnormalities Atrioventricular block Limb-girdle muscular dystrophy Lipodystrophy Mildly elevated creatine phosphokinase Difficulty climbing stairs Generalized hypotonia Congenital muscular dystrophy Coronary artery calcification Dilatation Pain Chest pain Ventricular tachycardia Intellectual disability Obesity Diabetes mellitus Infertility Hepatic steatosis Insulin resistance Decreased HDL cholesterol concentration Increased LDL cholesterol concentration Scoliosis Papule Arterial calcification Hypophosphatemic rickets Type 1 muscle fiber atrophy Restricted neck movement due to contractures Akinesia Tricuspid regurgitation Distal lower limb muscle weakness Increased variability in muscle fiber diameter Right bundle branch block Sprengel anomaly Bulbar palsy Proximal lower limb amyotrophy Hypokinesia Proximal upper limb amyotrophy Centrally nucleated skeletal muscle fibers Proximal muscle weakness in lower limbs Ventricular extrasystoles Atrial flutter Peroneal muscle atrophy Proximal muscle weakness in upper limbs Shoulder girdle muscle weakness Achilles tendon contracture Scapuloperoneal amyotrophy Cataract Delayed speech and language development Peripheral neuropathy Diarrhea Constipation Respiratory failure Vocal cord paralysis Distal muscle weakness Myofibrillar myopathy Distal lower limb amyotrophy Paresthesia Peroneal muscle weakness Generalized muscle weakness Left anterior fascicular block Muscle stiffness Limb-girdle muscle atrophy Restrictive cardiomyopathy Hyporeflexia of lower limbs Skeletal myopathy Knee flexion contracture Supraventricular arrhythmia Ankle contracture Waddling gait Ventricular escape rhythm Frequent falls Bradycardia Decreased cervical spine flexion due to contractures of posterior cervical muscles Reduced tendon reflexes Falls Ventricular arrhythmia Back pain Spinal muscular atrophy Myotonia Toe walking Marked muscular hypertrophy Calf muscle hypertrophy Abnormal atrioventricular conduction Atrial arrhythmia Ichthyosis Proximal spinal muscular atrophy Ptosis Right ventricular cardiomyopathy Intestinal pseudo-obstruction Sick sinus syndrome Third degree atrioventricular block Late-onset proximal muscle weakness Pica Proximal amyotrophy High palate Neonatal hypotonia Wide nasal bridge Kyphosis Midface retrusion Pectus excavatum Pes cavus Difficulty walking Rigidity Shoulder girdle muscle atrophy Restrictive heart failure Acanthosis nigricans Loss of gluteal subcutaneous adipose tissue Poor head control Talipes equinovarus Narrow chest Abnormality of the foot Joint hyperflexibility Talipes Limitation of joint mobility Decreased fetal movement EMG abnormality Severe muscular hypotonia Cachexia Growth delay Generalized amyotrophy Axial muscle weakness Short stature Hearing impairment Conductive hearing impairment Genu valgum Cyanosis Growth abnormality Glomerulosclerosis Motor delay Global developmental delay Hypophosphatemia Left ventricular noncompaction cardiomyopathy Dementia Abnormality of the cardiovascular system Abnormal EKG Myocardial fibrosis Cardiac arrest T-wave inversion Edema Myocarditis Left ventricular noncompaction Abnormality of the liver Cardiogenic shock Type II diabetes mellitus Azoospermia Hypercholesterolemia Oligospermia Premature coronary artery atherosclerosis Cardiomegaly Nephrocalcinosis Shock Tachypnea Ectopic calcification Rickets Pericardial effusion Abnormality of skeletal muscle fiber size Maternal diabetes Coronary artery atherosclerosis Reduced subcutaneous adipose tissue Lipoatrophy Aplasia/Hypoplasia of the skin Abnormality of the musculature Secondary amenorrhea Hyperuricemia Insulin-resistant diabetes mellitus Oligomenorrhea Preeclampsia Hyperglycemia Abnormality of the neck Prominent superficial veins Xanthomatosis Hyperlipoproteinemia Calf muscle pseudohypertrophy Loss of subcutaneous adipose tissue in limbs Dysmenorrhea Loss of facial adipose tissue Eclampsia Prominent veins on trunk Skeletal muscle hypertrophy Hyperinsulinemia Ankylosis Splenomegaly Endocardial fibroelastosis Arterial stenosis Otosclerosis Arteriosclerosis Angioid streaks of the fundus Coronary artery stenosis Vascular calcification Periarticular calcification Hepatomegaly Hepatosplenomegaly Polycystic ovaries Cirrhosis Hirsutism Amenorrhea Epidermal acanthosis Primary amenorrhea Thin skin Abnormality of the face Generalized hirsutism Pancreatitis Atherosclerosis Absent muscle fiber emerin



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