Congestive heart failure, and Bipolar affective disorder

Diseases related with Congestive heart failure and Bipolar affective disorder

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


Top matches:

High match MCLEOD NEUROACANTHOCYTOSIS SYNDROME


McLeod neuroacanthocytosis syndrome (MLS) is a form of neuroacanthocytosis (see this term) and is characterized clinically by a Huntington's disease-like phenotype with an involuntary hyperkinetic movement disorder, psychiatric manifestations and cognitive alterations, and biochemically by absence of the Kx antigen and by weak expression of the Kell antigens.

MCLEOD NEUROACANTHOCYTOSIS SYNDROME Is also known as mls|x-linked mcleod syndrome

Related symptoms:

  • Seizures
  • Short stature
  • Muscle weakness
  • Cognitive impairment
  • Anemia


SOURCES: ORPHANET OMIM MENDELIAN

More info about MCLEOD NEUROACANTHOCYTOSIS SYNDROME

High match CARNEY COMPLEX, TYPE 1; CNC1


Carney complex is an autosomal dominant multiple neoplasia syndrome characterized by cardiac, endocrine, cutaneous, and neural myxomatous tumors, as well as a variety of pigmented lesions of the skin and mucosae. Carney complex may simultaneously involve multiple endocrine glands, similar to classic MEN syndromes (MEN1; {131100} and MEN2; {171400}). Carney complex shows some similarities to McCune-Albright syndrome (MAS ), a sporadic condition that is also characterized by multiple endocrine and nonendocrine tumors, and shares skin abnormalities and some nonendocrine tumors with the lentiginoses and certain of the hamartomatoses, particularly Peutz-Jeghers syndrome (PJS ). Carney complex is often associated with the unusual large-cell calcifying Sertoli cell tumor and psammomatous melanotic schwannomas (Kirschner et al., 2000; Stratakis et al., 2001).

CARNEY COMPLEX, TYPE 1; CNC1 Is also known as lamb syndrome|myxoma, spotty pigmentation, and endocrine overactivity|carney myxoma-endocrine complex|car|carney syndrome|name syndrome

Related symptoms:

  • Neoplasm
  • Muscle weakness
  • Pain
  • Hypertension
  • Fever


SOURCES: OMIM MENDELIAN

More info about CARNEY COMPLEX, TYPE 1; CNC1

High match GAUCHER DISEASE TYPE 1


Gaucher disease type 1 is the chronic non-neurological form of Gaucher disease (GD; see this term) characterized by organomegaly, bone involvement and cytopenia.

GAUCHER DISEASE TYPE 1 Is also known as gaucher disease, juvenile and adult, cerebral|gd iii|gaucher disease, chronic neuronopathic type|non-cerebral juvenile gaucher disease|gaucher disease, subacute neuronopathic type

Related symptoms:

  • Seizures
  • Global developmental delay
  • Short stature
  • Scoliosis
  • Ataxia


SOURCES: ORPHANET OMIM MENDELIAN

More info about GAUCHER DISEASE TYPE 1

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Other less relevant matches:

Medium match JACOBSEN SYNDROME


Jacobsen syndrome is a multiple congenital anomaly/mental retardation (MCA/MR) contiguous gene syndrome caused by partial deletion of the long arm of chromosome 11.

JACOBSEN SYNDROME Is also known as monosomy 11qter|del(11)(q23.3)|distal deletion 11q|telomeric deletion 11q|distal monosomy 11q|del(11)(qter)|chromosome 11q deletion syndrome|partial 11q monosomy syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: OMIM ORPHANET MENDELIAN

More info about JACOBSEN SYNDROME

Low match FAMILIAL DYSKINESIA AND FACIAL MYOKYMIA


Familial dyskinesia and facial myokymia is a rare paroxysmal movement disorder, with childhood or adolescent onset, characterized by paroxysmal choreiform, dystonic, and myoclonic movements involving the limbs (mostly distal upper limbs), neck and/or face, which can progressively increase in both frequency and severity until they become nearly constant. Patients may also present with delayed motor milestones, perioral and periorbital dyskinesias, dysarthria, hypotonia, and weakness.

FAMILIAL DYSKINESIA AND FACIAL MYOKYMIA Is also known as fdfm

Related symptoms:

  • Intellectual disability
  • Generalized hypotonia
  • Motor delay
  • Hyperreflexia
  • Dysarthria


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about FAMILIAL DYSKINESIA AND FACIAL MYOKYMIA

Low match CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC 27; CMH27


CMH27 is a severe, early-onset cardiomyopathy with morphologic features of both dilated and hypertrophic disease, characterized by biventricular involvement and atypical distribution of hypertrophy. Heterozygotes are at increased risk of developing cardiomyopathy (Almomani et al., 2016).For a general phenotypic description and a discussion of genetic heterogeneity of hypertrophic cardiomyopathy, see CMH1 (OMIM ).An oligogenic form of hypertrophic cardiomyopathy, involving heterozygous mutations in the ALPK3, TTN (OMIM ), and MYL3 (OMIM ) genes has also been reported in 1 family.

Related symptoms:

  • Abnormal facial shape
  • Low-set ears
  • High palate
  • Cardiomyopathy
  • Edema


SOURCES: OMIM MENDELIAN

More info about CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC 27; CMH27

Low match WOLFF-PARKINSON-WHITE SYNDROME


A group of conditions in which HEART VENTRICLE activation by the atrial impulse is faster than the normal impulse conduction from the SINOATRIAL NODE. In these pre-excitation syndromes, atrial impulses often bypass the ATRIOVENTRICULAR NODE delay and travel via ACCESSORY CONDUCTING PATHWAYS connecting the atrium directly to the BUNDLE OF HIS.

WOLFF-PARKINSON-WHITE SYNDROME Is also known as wpw syndrome

Related symptoms:

  • Pain
  • Respiratory distress
  • Cardiomyopathy
  • Congestive heart failure
  • Arrhythmia


SOURCES: OMIM ORPHANET MENDELIAN

More info about WOLFF-PARKINSON-WHITE SYNDROME

Low 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

Low match ACERULOPLASMINEMIA


Aceruloplasminemia is an adult-onset disorder of neurodegeneration with brain iron accumulation (NBIA; see this term) characterized by anemia, retinal degeneration, diabetes and various neurological symptoms.

ACERULOPLASMINEMIA Is also known as hereditary ceruloplasmin deficiency

Related symptoms:

  • Ataxia
  • Spasticity
  • Cognitive impairment
  • Anemia
  • Delayed speech and language development


SOURCES: OMIM ORPHANET MENDELIAN

More info about ACERULOPLASMINEMIA

Top 5 symptoms//phenotypes associated to Congestive heart failure and Bipolar affective disorder

Symptoms // Phenotype % cases
Arrhythmia Uncommon - Between 30% and 50% cases
Depressivity Uncommon - Between 30% and 50% cases
Dementia Uncommon - Between 30% and 50% cases
Dyspnea Uncommon - Between 30% and 50% cases
Anxiety Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Cardiomyopathy Chorea Dysarthria Cognitive impairment Spasticity Confusion Involuntary movements Dilated cardiomyopathy Cardiac arrest Parkinsonism Rigidity Palpitations Seizures Ataxia Tachycardia Cerebral atrophy Pain Respiratory distress Dystonia Behavioral abnormality Anemia Hypertonia Fatigue Osteoporosis Short stature

Rare Symptoms - Less than 30% cases


Carcinoma Hypertension Global developmental delay Edema Pheochromocytoma Hypertrophic cardiomyopathy Cardiomegaly Paraganglioma Muscle fibrillation Heart murmur Stroke Abnormality of the eye Recurrent respiratory infections Growth delay Bruising susceptibility Hypothyroidism Low-set ears Abnormal facial shape Generalized hypotonia Intellectual disability Supranuclear gaze palsy Increased serum ferritin Pancytopenia Syncope Cirrhosis Failure to thrive Neurological speech impairment Osteopenia Myoclonus Orofacial dyskinesia Tremor Thrombocytopenia Difficulty walking Motor delay Strabismus Neoplasm Scoliosis Abnormal heart morphology Dyskinesia Hepatomegaly Abnormality of movement Ventricular arrhythmia Gait disturbance Dysphagia Memory impairment Ventricular fibrillation Neuronal loss in central nervous system Insomnia Atrial fibrillation Emotional lability Left ventricular hypertrophy Hepatosplenomegaly Splenomegaly Babinski sign Muscle weakness Supraventricular tachycardia Hyperhidrosis Personality changes Sinusitis Short toe Tachypnea Decreased serum ceruloplasmin Leukodystrophy Azoospermia Aortic valve stenosis Holoprosencephaly Abnormal palate morphology Spina bifida Bone marrow hypocellularity Horseshoe kidney Multicystic kidney dysplasia Infantile muscular hypotonia Hand polydactyly Refractory anemia Transposition of the great arteries Mitral stenosis Ectopic anus Duodenal atresia Eyelid coloboma Chronic constipation Retinal dysplasia Diastasis recti Missing ribs Double outlet right ventricle Abnormal eyelash morphology Wheezing Natal tooth Schizophrenia Slender finger Partial agenesis of the corpus callosum Atrioventricular canal defect Hypoplastic left heart Aplasia/Hypoplasia of the eyebrow Flat occiput Hammertoe Chorioretinal coloboma Ectropion Trigonocephaly Pyloric stenosis Short thumb Eczema Amblyopia Intellectual disability, moderate Finger syndactyly Skin rash Attention deficit hyperactivity disorder Abnormal cardiac septum morphology Coloboma Craniosynostosis Postnatal growth retardation Feeding difficulties in infancy Camptodactyly Low-set, posteriorly rotated ears Telecanthus Small for gestational age Hydronephrosis Hypoglycemia Thin upper lip vermilion Pes planus Retrognathia High forehead Hypogonadism Prominent forehead Agenesis of corpus callosum Constipation Leukemia Hip dislocation Pachygyria Intestinal malrotation Abnormal form of the vertebral bodies Coarctation of aorta Nuclear cataract Dehydration Microdontia Otitis media Growth hormone deficiency Webbed neck Decreased antibody level in blood Elevated hepatic iron concentration Premature birth Dolichocephaly Postural instability Microcornea Single transverse palmar crease Iris coloboma Anal atresia Decreased serum iron Smooth philtrum Talipes Facial asymmetry Narrow chest Toe syndactyly Broad hallux phalanx Pulmonary edema Aplasia/Hypoplasia of the earlobes Ventricular preexcitation with multiple accessory pathways Gait ataxia Pulsatile tinnitus Recurrent paroxysmal headache Gastrointestinal stroma tumor Renal cell carcinoma Poor speech Neuroblastoma Cranial nerve paralysis Headache Paroxysmal supraventricular tachycardia Delayed speech and language development Ventricular preexcitation Shortened PR interval Prolonged QRS complex Paroxysmal atrial fibrillation Atrial flutter Wolff-Parkinson-White syndrome Atrioventricular block Hypotension Chest pain Sudden cardiac death Diabetes mellitus Episodic paroxysmal anxiety Multiple pterygia Skeletal muscle atrophy Frontotemporal dementia Global brain atrophy Agitation Amyotrophic lateral sclerosis Apathy Respiratory insufficiency due to muscle weakness Stereotypy Aggressive behavior Cerebral cortical atrophy Respiratory insufficiency Elevated urinary catecholamines Adrenal pheochromocytoma Paraganglioma of head and neck Glomus jugular tumor Extraadrenal pheochromocytoma Disinhibition Primitive reflex Perseveration Chemodectoma Bulimia Semantic dementia Hypertension associated with pheochromocytoma Vertigo Left ventricular noncompaction Labial hypoplasia Toe clinodactyly Megakaryocyte dysplasia Congenital thrombocytopenia Bilateral camptodactyly Cogwheel rigidity Arteria lusoria Internal hemorrhage Annular pancreas Abnormality of the anus Scanning speech Giant platelets Blepharospasm Macular hypoplasia Clitoral hypoplasia Central hypothyroidism U-Shaped upper lip vermilion Urethral stenosis Abnormal lower motor neuron morphology Abnormality of the head Nasolacrimal duct obstruction Broad columella Abnormal thrombocyte morphology Abnormality of the curvature of the vertebral column Hyperreflexia Right ventricular hypertrophy Myokymia Retinal degeneration Tricuspid regurgitation Pterygium Hydrops fetalis Ventricular hypertrophy Neurodegeneration Abnormality of extrapyramidal motor function High palate Facial myokymia Paroxysmal dyskinesia Limb hypertonia Polyuria Resting tremor Delayed gross motor development Type I diabetes mellitus Clinodactyly of the 5th finger Torticollis Cerebral palsy Choreoathetosis Muscular hypotonia of the trunk Hyperkinesis Slurred speech Long hallux Sensorineural hearing impairment Inguinal hernia Growth hormone excess Multiple lentigines Red hair Schwannoma Thyroid carcinoma Generalized hypopigmentation Pituitary adenoma Macroorchidism Blue irides Increased circulating cortisol level Striae distensae Pituitary prolactin cell adenoma Freckling Macule Neurofibromas Hypermelanotic macule Precocious puberty Sarcoma Ischemic stroke Hemangioma Increased body weight Gynecomastia Fibroma Testicular neoplasm Tall stature Abdominal pain Ascites Hematuria Abnormality of skin pigmentation Lymphadenopathy Abnormality of eye movement Delayed puberty Corneal opacity Proteinuria Arthritis EEG abnormality Delayed skeletal maturation Follicular hyperplasia Kyphosis Diarrhea Myopia Cutaneous myxoma Myxoid subcutaneous tumors Thyroid follicular hyperplasia Profuse pigmented skin lesions Cardiac myxoma Uterine leiomyoma Follicular thyroid carcinoma Cafe-au-lait spot Abnormality of the skin Abnormal bleeding Generalized-onset seizure Restlessness Impaired pain sensation Impaired vibration sensation in the lower limbs Rhabdomyolysis Bowel incontinence Sensory axonal neuropathy Obsessive-compulsive behavior Sleep apnea Sensorimotor neuropathy Hallucinations Sensory neuropathy Left bundle branch block Hemolytic anemia Paresthesia Lower limb muscle weakness Abnormality of the cerebral white matter Mental deterioration Elevated hepatic transaminase Elevated serum creatine phosphokinase Areflexia Myopathy Peripheral neuropathy Ventricular extrasystoles Motor axonal neuropathy Nevus Recurrent singultus Hirsutism Papule Myalgia Proximal muscle weakness Weight loss Fever Abnormality of the astrocytes Hyporeflexia of upper limbs Abnormal facial expression Blood group antigen abnormality Abnormal corpus striatum morphology Acanthocytosis Caudate atrophy Abnormal lactate dehydrogenase activity Abnormal social behavior Impaired temperature sensation Generalized limb muscle atrophy Personality disorder Increased muscle fatiguability Hyporeflexia of lower limbs Excessive salivation Tics Abdominal distention Generalized myoclonic seizures Patent ductus arteriosus Hypertelorism Brachydactyly Epicanthus Depressed nasal bridge Feeding difficulties Flexion contracture Ptosis Cryptorchidism Cataract Muscular hypotonia Micrognathia Microcephaly Intrauterine growth retardation Hearing impairment Horizontal supranuclear gaze palsy Cardiac valve calcification Hematological neoplasm Decreased beta-glucocerebrosidase protein and activity Puberty and gonadal disorders Biliary tract obstruction Vascular calcification Erlenmeyer flask deformity of the femurs Orthopnea Wide nasal bridge Macrocephaly Arthralgia of the hip Short nose Clinodactyly Pectus excavatum Hypospadias Hernia Abnormality of cardiovascular system morphology Recurrent infections Microphthalmia Immunodeficiency Syndactyly Long philtrum Intellectual disability, mild Optic atrophy Abnormality of the dentition Atrial septal defect Hydrocephalus Short neck Anteverted nares Ventriculomegaly Talipes equinovarus Ventricular septal defect Frontal bossing Downslanted palpebral fissures Abnormal platelet function Flank pain Cyanosis Meningitis Clubbing Abnormality of the thorax Portal hypertension Cholelithiasis Increased susceptibility to fractures Reduced bone mineral density Leukopenia Oculomotor apraxia Osteolysis Spastic paraparesis Increased bone mineral density Menorrhagia Bone pain Hepatic fibrosis Anorexia Decreased body weight Osteoarthritis Progressive neurologic deterioration Epistaxis Pulmonary arterial hypertension Apraxia Abnormality of the cardiovascular system Leukocytosis Osteomyelitis Abnormality of bone marrow cell morphology Vertebral compression fractures Spontaneous hematomas Fractures of the long bones Hypersplenism Esodeviation Periorbital edema Generalized osteosclerosis Abnormality of the spleen Avascular necrosis of the capital femoral epiphysis Abnormal myocardium morphology Multiple myeloma Edema of the lower limbs Increased antibody level in blood Hepatocellular carcinoma Gingival bleeding Protuberant abdomen Aseptic necrosis Exertional dyspnea Pathologic fracture Interstitial pulmonary abnormality Pericardial effusion Petechiae Abnormality of coagulation Aceruloplasminemia



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