Congestive heart failure, and Headache

Diseases related with Congestive heart failure and Headache

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


Top matches:

Medium match VEIN OF GALEN ANEURYSMAL MALFORMATION


Vein of Galen aneurysmal malformation (VGAM) is a congenital vascular malformation characterized by dilation of the embryonic precursor of the vein of Galen. It is a sporadic lesion that occurs during embryogenesis.

VEIN OF GALEN ANEURYSMAL MALFORMATION Is also known as vein of galen arteriovenous malformations

Related symptoms:

  • Congestive heart failure
  • Headache
  • Dilatation
  • Abnormality of the cerebral vasculature
  • Prominent superficial veins


SOURCES: MESH ORPHANET MENDELIAN

More info about VEIN OF GALEN ANEURYSMAL MALFORMATION

Medium match PARKES WEBER SYNDROME


Related symptoms:

  • Congestive heart failure
  • Headache
  • Glaucoma
  • Abnormal bleeding
  • Hemiparesis


SOURCES: ORPHANET MENDELIAN

More info about PARKES WEBER SYNDROME

Medium match INFANTILE HYPERTROPHIC CARDIOMYOPATHY DUE TO MRPL44 DEFICIENCY


Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency is a rare mitochondrial oxidative phosphorylation disorder with complex I and IV deficiency characterized by hypertrophic cardiomyopathy, hepatic steatosis with elevated liver transaminases, exercise intolerance and muscle weakness. Neuro-opthalmological features (hemiplegic migraine, Leigh-like lesions on brain MRI, pigmentary retinopathy) have been reported later in life.

INFANTILE HYPERTROPHIC CARDIOMYOPATHY DUE TO MRPL44 DEFICIENCY Is also known as combined oxidative phosphorylation defect type 16|coxpd16

Related symptoms:

  • Cardiomyopathy
  • Congestive heart failure
  • Headache
  • Elevated hepatic transaminase
  • Hypertrophic cardiomyopathy


SOURCES: ORPHANET OMIM MENDELIAN

More info about INFANTILE HYPERTROPHIC CARDIOMYOPATHY DUE TO MRPL44 DEFICIENCY

Mendelian

Too many results?
We can help you with your rare disease diagnosis.

Learn more

Other less relevant matches:

Medium match ACQUIRED IDIOPATHIC SIDEROBLASTIC ANEMIA


Acquired idiopathic sideroblastic anaemia is one of a group of disorders known as the myelodysplastic syndromes (MDS) characterised by ineffective haemopoiesis affecting one or more blood cell lineages (myeloid, erythroid or megakaryocytic) leading to peripheral blood cytopenias and an increased risk of developing leukaemia. Acquired idiopathic sideroblastic anaemia is now more commonly referred to as refractory anaemia with ringed sideroblasts or the acronym RARS.

ACQUIRED IDIOPATHIC SIDEROBLASTIC ANEMIA Is also known as rars|primary acquired sideroblastic anemia|refractory anemia with ringed sideroblasts|aisa

Related symptoms:

  • Pain
  • Anemia
  • Fatigue
  • Respiratory distress
  • Congestive heart failure


SOURCES: OMIM ORPHANET MENDELIAN

More info about ACQUIRED IDIOPATHIC SIDEROBLASTIC ANEMIA

Medium match PARAGANGLIOMAS 4; PGL4


PARAGANGLIOMAS 4; PGL4 Is also known as paraganglioma, familial malignant|pheochromocytoma, extraadrenal, and cervical paraganglioma|carotid body tumors and multiple extraadrenal pheochromocytomas|pheochromocytoma, familial extraadrenal|paragangliomas, hereditary extraadrenal

Related symptoms:

  • Neoplasm
  • Pain
  • Hypertension
  • Congestive heart failure
  • Headache


SOURCES: OMIM MENDELIAN

More info about PARAGANGLIOMAS 4; PGL4

Medium match CEREBRAL CAVERNOUS MALFORMATIONS; CCM


Cerebral cavernous angiomas are relatively rare vascular malformations that may involve any part of the central nervous system. Cerebral cavernous angiomas are to be distinguished from cerebral arteriovenous malformations ({106070}, {108010}). CCMs are venous and not demonstrable by arteriography; hence they are referred to as angiographically silent.Capillary hemangiomas (OMIM ) are classified as distinct from vascular malformations in that hemangiomas are benign, highly proliferative lesions involving aberrant localized growth of capillary endothelium. Hemangiomas develop shortly after birth. In contrast, vascular malformations are present from birth, tend to grow with the individual, do not regress, and show normal rates of endothelial cell turnover (Mulliken and Young, 1988). Genetic Heterogeneity of CCMCCM2 (OMIM ) is caused by mutation in the CCM2/malcavernin gene (OMIM ), and CCM3 (OMIM ) is caused by mutation in the PDCD10 gene (OMIM ).Evidence suggests that a 2-hit mechanism involving biallelic germline and somatic mutations is responsible for CCM1 pathogenesis, see PATHOGENESIS and MOLECULAR GENETICS sections.

CEREBRAL CAVERNOUS MALFORMATIONS; CCM Is also known as cam|cerebral capillary malformations|cavernous angiomatous malformations|cavernous angioma, familial

Related symptoms:

  • Seizures
  • Muscle weakness
  • Hepatomegaly
  • Congestive heart failure
  • Headache


SOURCES: ORPHANET OMIM MENDELIAN

More info about CEREBRAL CAVERNOUS MALFORMATIONS; CCM

Low match FAMILIAL ATRIAL MYXOMA


Familial atrial myxoma is a rare, genetic cardiac tumor characterized by the presence of a primary, benign, gelatinous mass located in the atria and composed of primitive connective tissue cells and stroma (resembling mesenchyme) in several members of a family. Clinical presentation depends on the size, mobility and location of tumor, ranging from nonspecific and/or constitutional symptoms to sudden cardiac death, and includes dyspnea, hemoptisis, syncope, fatigue, fever, cutaneous rash, increases in venous pressure and/or peripheral edema.

FAMILIAL ATRIAL MYXOMA Is also known as atrial myxoma, familial

Related symptoms:

  • Seizures
  • Cognitive impairment
  • Fever
  • Atrial septal defect
  • Congestive heart failure


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about FAMILIAL ATRIAL MYXOMA

Low match HEREDITARY HEMORRHAGIC TELANGIECTASIA


Rendu-Osler-Weber disease, also called hereditary hemorrhagic telangiectasia (HHT), is a disorder of angiogenesis leading to arteriovenous dilatations: cutaneo-mucosal hemorrhagic telangiectasias and visceral shunting.

HEREDITARY HEMORRHAGIC TELANGIECTASIA Is also known as hht|rendu-osler disease|rendu-osler-weber disease

Related symptoms:

  • Seizures
  • Congestive heart failure
  • Cirrhosis
  • Hepatic failure
  • Hematuria


SOURCES: ORPHANET MENDELIAN

More info about HEREDITARY HEMORRHAGIC TELANGIECTASIA

Low match JUVENILE POLYPOSIS SYNDROME; JPS


Juvenile polyposis syndrome is an autosomal dominant condition that predisposes gene carriers to various types of tumors. The diagnosis is based on the occurrence of hamartomatous gastrointestinal polyps that turn into malignant lesions in approximately 20% of cases (Handra-Luca et al., 2005).It had been suggested that juvenile polyposis can be caused by mutations in the PTEN gene (OMIM ), the same gene that is mutant in Cowden syndrome-1 (OMIM ). In a comprehensive review of PTEN, Waite and Eng (2002) concluded that juvenile intestinal polyposis is not a so-called PTEN hamartoma-tumor syndrome (PHTS). They suggested that the discovery of the germline PTEN mutation in an individual considered to have JPS should raise a suspicion that the clinical diagnosis is incorrect and that such an individual should be managed medically in the same manner as all patients with PHTS.

JUVENILE POLYPOSIS SYNDROME; JPS Is also known as polyposis, juvenile intestinal|pji|jip|juvenile intestinal polyposis|polyposis, familial, of entire gastrointestinal tract

Related symptoms:

  • Seizures
  • Neoplasm
  • Failure to thrive
  • Pain
  • Cryptorchidism


SOURCES: OMIM MENDELIAN

More info about JUVENILE POLYPOSIS SYNDROME; JPS

Low match TSH-SECRETING PITUITARY ADENOMA


A rare adenoma of the anterior lobe of the pituitary gland that produces thyrotropin. It is usually associated with goiter and hyperthyroidism.

TSH-SECRETING PITUITARY ADENOMA Is also known as thyrotroph adenoma|pituitary thyrotrophic adenoma|thyroid stimulating hormone-secreting pituitary adenoma|tsh-oma

Related symptoms:

  • Seizures
  • Ptosis
  • Hypertension
  • Tremor
  • Fatigue


SOURCES: ORPHANET MENDELIAN

More info about TSH-SECRETING PITUITARY ADENOMA

Top 5 symptoms//phenotypes associated to Congestive heart failure and Headache

Symptoms // Phenotype % cases
Seizures Uncommon - Between 30% and 50% cases
Chest pain Uncommon - Between 30% and 50% cases
Fatigue Uncommon - Between 30% and 50% cases
Palpitations Uncommon - Between 30% and 50% cases
Pain Uncommon - Between 30% and 50% cases
Mendelian

Accelerate your rare disease diagnosis with us

Learn more

Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Hypertension Cerebral hemorrhage Peripheral arteriovenous fistula

Rare Symptoms - Less than 30% cases


Easy fatigability Cranial nerve paralysis Epistaxis Gastrointestinal hemorrhage Intestinal polyposis Microcytic anemia Neoplasm Subarachnoid hemorrhage Hyperhidrosis Carcinoma Portal hypertension Vertigo Growth hormone excess Stroke Migraine Telangiectasia Pallor Cavernous hemangioma Hepatic vascular malformations Jaundice Hypokalemia Diplopia Tachycardia Hemoptysis Cardiomegaly Paralysis Respiratory distress Anemia Dilatation Abnormality of the cerebral vasculature Telangiectasia of the skin Oculomotor nerve palsy Umbilical hernia Cough Enlarged pituitary gland Cyanosis Cranial nerve VI palsy Hypoalbuminemia Clubbing Colon cancer Euthyroid hyperthyroxinemia Fourth cranial nerve palsy Hamartoma Polycythemia Hematochezia Abnormality of the pituitary gland Clubbing of fingers Rectal prolapse Stomach cancer Dyspnea Macrocephaly Abdominal pain Spontaneous hematomas Pulmonary embolism Transient ischemic attack Arteriovenous malformation Esophageal varix Heteronymous hemianopia Visceral angiomatosis Conjunctival telangiectasia Cholecystitis Abnormality of cardiovascular system physiology Hernia Mucosal telangiectasiae Retinal telangiectasia Failure to thrive Abnormality of hair density Abnormal visual field test Internal ophthalmoplegia Cryptorchidism Hematemesis Diarrhea Hamartomatous polyposis Intussusception Periodic hypokalemic paresis Decreased circulating ACTH level Ventricular arrhythmia Goiter Impotence Pericardial effusion Hyperthyroidism Central adrenal insufficiency Increased circulating gonadotropin level Increased thyroid-stimulating hormone level Sudden loss of visual acuity Gynecomastia Prolactin excess Male hypogonadism Adrenocorticotropic hormone deficiency Menstrual irregularities Hemianopia Supraventricular arrhythmia Abnormality of the menstrual cycle Decreased female libido Decreased fertility in females Hypogonadotrophic hypogonadism Progressive visual loss Melena Decreased fertility in males Secondary growth hormone deficiency Erectile abnormalities Multiple gastric polyps Duodenal adenocarcinoma Bitemporal hemianopia Adenocarcinoma of the colon Ptosis Tremor Blindness Hypotension Adrenocorticotropin deficient adrenal insufficiency Vomiting Osteoporosis Female hypogonadism Hypogonadism Weight loss Osteopenia Delayed puberty Infertility Nausea and vomiting Edema of the lower limbs Cholelithiasis Pheochromocytoma Decreased mean corpuscular volume Sideroblastic anemia Abnormal glucose tolerance Hypochromic anemia Crackles Refractory sideroblastic anemia Anxiety Neuroblastoma Renal cell carcinoma Paraganglioma Irritability Gastrointestinal stroma tumor Recurrent paroxysmal headache Pulsatile tinnitus Episodic paroxysmal anxiety Adrenal pheochromocytoma Hypertension associated with pheochromocytoma Chemodectoma Extraadrenal pheochromocytoma Glomus jugular tumor Increased serum ferritin Hepatosplenomegaly Elevated urinary catecholamines Hypertrophy of the lower limb Prominent superficial veins Increased head circumference Vein of Galen aneurysmal malformation Glaucoma Abnormal bleeding Hemiparesis Nevus flammeus Varicose veins Vascular skin abnormality Hypertrophy of the upper limb Arrhythmia Cardiomyopathy Elevated hepatic transaminase Hypertrophic cardiomyopathy Respiratory tract infection Hepatic steatosis Increased serum lactate Abnormality of mitochondrial metabolism Microvesicular hepatic steatosis Decreased activity of mitochondrial respiratory chain Paraganglioma of head and neck Muscle weakness Venous thrombosis Orthopnea Neoplasm of the skin Ischemic stroke Heart murmur Tricuspid regurgitation Exertional dyspnea Thromboembolism Dilatation of the cerebral artery Pulmonary edema Endocarditis Increased inflammatory response Mitral valve prolapse Bacterial endocarditis Cardiac myxoma Pulmonic valve myxoma Cirrhosis Hepatic failure Hematuria Pulmonary arterial hypertension Nephrolithiasis Amblyopia Cholestasis Syncope Hepatomegaly Venous malformation Lower limb muscle weakness Abnormality of the skin Focal-onset seizure Cerebral calcification Hemangioma Intracranial hemorrhage Abnormality of the musculature Capillary hemangioma Neuritis Varicocele Ascites Retrobulbar optic neuritis Retinal vascular malformation Cognitive impairment Fever Atrial septal defect Behavioral abnormality Confusion Abnormality of skin pigmentation Coma Thyroid crisis



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Microphthalmia and Palmoplantar keratoderma, related diseases and genetic alterations Ventricular septal defect and Long philtrum, related diseases and genetic alterations

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more