Congestive heart failure, and Neoplasm of the pancreas

Diseases related with Congestive heart failure and Neoplasm of the pancreas

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


Top matches:

Medium match CARNEY COMPLEX


Carney complex (CNC) is characterized by spotty skin pigmentation, endocrine overactivity and myxomas.

CARNEY COMPLEX Is also known as myxoma-spotty pigmentation-endocrine overactivity syndrome|carney syndrome|carney myxoma-endocrine complex, type 2

Related symptoms:

  • Neoplasm
  • Congestive heart failure
  • Stroke
  • Hirsutism
  • Sudden cardiac death


SOURCES: ORPHANET OMIM MENDELIAN

More info about CARNEY COMPLEX

Medium match TUBEROUS SCLEROSIS COMPLEX


Tuberous sclerosis complex (TSC) is a neurocutaneous disorder characterized by multisystem hamartomas and associated with neuropsychiatric features.

TUBEROUS SCLEROSIS COMPLEX Is also known as tuberous sclerosis|bourneville syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Neoplasm
  • Cognitive impairment


SOURCES: OMIM ORPHANET MENDELIAN

More info about TUBEROUS SCLEROSIS COMPLEX

Low match CONGENITAL ATRANSFERRINEMIA


Congenital atransferrinemia is a very rare hematologic disease caused by a transferrin (TF) deficiency and characterized by microcytic, hypochromic anemia (manifesting with pallor, fatigue and growth retardation) and iron overload, and that can be fatal if left untreated.

CONGENITAL ATRANSFERRINEMIA Is also known as hypotransferrinemia, familial|congenital hypotransferrinemia

Related symptoms:

  • Growth delay
  • Anemia
  • Hepatomegaly
  • Fatigue
  • Congestive heart failure


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about CONGENITAL ATRANSFERRINEMIA

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Other less relevant matches:

Low match HEMOCHROMATOSIS TYPE 2


Hemochromatosis type 2 (juvenile) is the early-onset and most severe form of rare hereditary hemochromatosis (HH; see this term), a group of diseases characterized by excessive tissue iron deposition of genetic origin.

HEMOCHROMATOSIS TYPE 2 Is also known as juvenile hemochromatosis

Related symptoms:

  • Muscle weakness
  • Pain
  • Hypertension
  • Hepatomegaly
  • Cardiomyopathy


SOURCES: OMIM ORPHANET MENDELIAN

More info about HEMOCHROMATOSIS TYPE 2

Low match SECKEL SYNDROME 10; SCKL10


Related symptoms:

  • Short stature
  • Microcephaly
  • Micrognathia
  • Abnormal facial shape
  • Hypertension


SOURCES: OMIM MENDELIAN

More info about SECKEL SYNDROME 10; SCKL10

Low match NEUTRAL LIPID STORAGE MYOPATHY


Neutral lipid storage disease with myopathy is an autosomal recessive muscle disorder characterized by adult onset of slowly progressive proximal muscle weakness affecting the upper and lower limbs and associated with increased serum creatine kinase; distal muscle weakness may also occur. About half of patients develop cardiomyopathy later in the disease course. Other variable features include diabetes mellitus, hepatic steatosis, hypertriglyceridemia, and possibly sensorineural hearing loss. Leukocytes and muscle cells show cytoplasmic accumulation of triglycerides (summary by Reilich et al., 2011).Neutral lipid storage disease with myopathy belongs to a group of disorders termed neutral lipid storage disorders (NLSDs). These disorders are characterized by the presence of triglyceride-containing cytoplasmic droplets in leukocytes and in other tissues, including bone marrow, skin, and muscle. Chanarin-Dorfman syndrome (CDS ) is defined as NLSD with ichthyosis (NLSDI). Patients with NLSDM present with myopathy but without ichthyosis (summary by Fischer et al., 2007).

NEUTRAL LIPID STORAGE MYOPATHY Is also known as neutral lipid storage disease with myopathy without ichthyosis|nlsdm|triglyceride deposit cardiomyovasculopathy|neutral lipid storage disease without ichthyosis

Related symptoms:

  • Short stature
  • Generalized hypotonia
  • Hearing impairment
  • Sensorineural hearing impairment
  • Muscle weakness


SOURCES: ORPHANET OMIM MENDELIAN

More info about NEUTRAL LIPID STORAGE MYOPATHY

Low match AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE


Autosomal recessive polycystic kidney disease (ARPKD) is an inherited disorder characterised by the development of cysts affecting the collecting ducts. It is frequently associated with hepatic involvement.

AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE Is also known as polycystic kidney and hepatic disease 1|polycystic kidney disease, infantile, type i|pkhd1|arpkd|ar-pkd|polycystic kidney disease, autosomal recessive|polycystic kidney disease 4 with or without hepatic disease|pkd3, formerly

Related symptoms:

  • Micrognathia
  • Hypertension
  • Hepatomegaly
  • Ventricular septal defect
  • Respiratory insufficiency


SOURCES: OMIM ORPHANET MENDELIAN

More info about AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE

Low match SYMPTOMATIC FORM OF HEMOCHROMATOSIS TYPE 1


Symptomatic form of hemochromatosis type 1 is a rare, hereditary hemochromatosis characterized by inappropriately regulated intestinal iron absorption which leads to excessive iron storage in various organs and manifests with a wide range of signs and symptoms, including abdominal pain, weakness, lethargy, weight loss, elevated serum aminotransferase levels, increase in skin pigmentation, and/or arthropathy in the metacarpophalangeal joints. Other commonly associated manifestations include hepatomegaly, cirrhosis, liver fibrosis, hepatocellular carcinoma, restrictive cardiomyopathy and/or diabetes mellitus.

SYMPTOMATIC FORM OF HEMOCHROMATOSIS TYPE 1 Is also known as symptomatic form of hfe-related hereditary hemochromatosis|symptomatic form of classic hemochromatosis

Related symptoms:

  • Peripheral neuropathy
  • Hepatomegaly
  • Fatigue
  • Cardiomyopathy
  • Congestive heart failure


SOURCES: ORPHANET MENDELIAN

More info about SYMPTOMATIC FORM OF HEMOCHROMATOSIS TYPE 1

Low 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

Low match AUTOSOMAL SEMI-DOMINANT SEVERE LIPODYSTROPHIC LAMINOPATHY


Related symptoms:

  • Micrognathia
  • Hepatomegaly
  • Myopathy
  • Congestive heart failure
  • Splenomegaly


SOURCES: ORPHANET MENDELIAN

More info about AUTOSOMAL SEMI-DOMINANT SEVERE LIPODYSTROPHIC LAMINOPATHY

Top 5 symptoms//phenotypes associated to Congestive heart failure and Neoplasm of the pancreas

Symptoms // Phenotype % cases
Hepatomegaly Common - Between 50% and 80% cases
Diabetes mellitus Common - Between 50% and 80% cases
Hepatic steatosis Uncommon - Between 30% and 50% cases
Splenomegaly 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 Neoplasm of the pancreas. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Abnormality of the liver Cirrhosis Hypertriglyceridemia Cardiomyopathy Myopathy Acanthosis nigricans Insulin resistance Fatigue Myalgia Micrognathia Polycystic ovaries Dilatation

Rare Symptoms - Less than 30% cases


Osteoporosis Hypogonadism Elevated hepatic transaminase Neoplasm Muscle weakness Pain Amenorrhea Scarring Arthritis Recurrent infections Abnormality of the pancreas Skin tags Multiple renal cysts Renal cyst Hypothyroidism Arrhythmia Infertility Increased serum ferritin Hyperpigmentation of the skin Lipodystrophy Dysmenorrhea Loss of subcutaneous adipose tissue in limbs Decreased HDL cholesterol concentration Xanthomatosis Secondary amenorrhea Aplasia/Hypoplasia of the skin Lipoatrophy Reduced subcutaneous adipose tissue Coronary artery atherosclerosis Skeletal muscle hypertrophy Atherosclerosis Portal hypertension Pancreatitis Generalized hirsutism Thin skin Hypertrophic cardiomyopathy Cholestasis Hepatosplenomegaly Insulin-resistant diabetes mellitus Short stature Congenital hepatic fibrosis Respiratory insufficiency Arthropathy Renal insufficiency Impotence Hirsutism Subcutaneous nodule Cafe-au-lait spot Chronic lung disease Pulmonary hypoplasia Dehydration Oligohydramnios Depressed nasal ridge Thyroid carcinoma Abnormal lung morphology Hepatic fibrosis Renal hypoplasia/aplasia Chronic kidney disease Polycystic kidney dysplasia Enlarged kidney Motor delay Abnormality of the kidney Hypersplenism Absence of renal corticomedullary differentiation Azotemia Hypoplasia of the ear cartilage Periportal fibrosis Potter facies Hematemesis Portal fibrosis Atelectasis Biliary tract abnormality Tubulointerstitial fibrosis Hepatic cysts Pancreatic cysts Cholangitis Esophageal varix Stage 5 chronic kidney disease Low-set, posteriorly rotated ears Alopecia Ovarian cyst Hearing impairment Sensorineural hearing impairment Skeletal muscle atrophy Hypoplasia of the musculature Obesity Areflexia Elevated serum creatine phosphokinase Difficulty walking Proximal muscle weakness Stomach cancer Distal muscle weakness Ichthyosis Waddling gait Progressive muscle weakness Fasciculations Parathyroid adenoma Exercise intolerance Hyperlipidemia Easy fatigability Psoriasiform dermatitis Gowers sign Difficulty running Neck muscle weakness Progressive proximal muscle weakness Increased muscle lipid content Ventricular septal defect Respiratory distress Atrial septal defect Respiratory failure Macrotia Peripheral neuropathy Vertigo Arthralgia Progeroid facial appearance Hyperlipoproteinemia Calf muscle pseudohypertrophy Stroke Loss of facial adipose tissue Eclampsia Prominent veins on trunk Abnormality of skeletal muscle fiber size Loss of gluteal subcutaneous adipose tissue Marked muscular hypertrophy Round face Abnormality of the nail Ventricular arrhythmia Premature graying of hair Osteolytic defects of the phalanges of the hand Nevus Precocious atherosclerosis Advanced eruption of teeth Supraventricular arrhythmia Abnormal atrioventricular conduction Narrow nasal ridge Decreased serum leptin Accelerated atherosclerosis Increased adipose tissue around the neck Minimal subcutaneous fat Acroosteolysis of distal phalanges (feet) Increased intraabdominal fat Decreased adiponectin level Increased facial adipose tissue Muscle hypertrophy of the lower extremities Sudden cardiac death Prominent superficial veins Retinopathy Pituitary adenoma Elevated serum alanine aminotransferase Ascites Limitation of joint mobility Gynecomastia Joint dislocation Hepatocellular carcinoma Exocrine pancreatic insufficiency Chondrocalcinosis Abnormality of the hypothalamus-pituitary axis Neoplasm of the endocrine system Epidermal acanthosis Myocardial infarction Primary amenorrhea Abnormality of the face Abnormality of the neck Prolactin excess Increased circulating cortisol level Growth hormone excess Hyperinsulinemia Hyperglycemia Ovarian neoplasm Colon cancer Hypermelanotic macule Neoplasm of the skin Abnormality of the musculature Hyperuricemia Oligomenorrhea Maternal diabetes Preeclampsia Generalized hypotonia Elevated serum aspartate aminotransferase Optic atrophy Shagreen patch Gingivitis Pigmentation of the sclera Abnormality of the respiratory system Wolff-Parkinson-White syndrome Abnormal pigmentation of the oral mucosa Astrocytoma Gingival fibromatosis Pneumothorax Rhabdomyosarcoma Abnormality of the pleura Chylothorax Adenoma sebaceum Third degree atrioventricular block Ependymoma Macrodactyly Nevus flammeus Optic nerve glioma Renal angiomyolipoma Angiofibromas Retinal hamartoma Chordoma Cortical tubers Subependymal nodules Cardiac rhabdomyoma Hypomelanotic macule Dental enamel pits Ungual fibroma Confetti-like hypopigmented macules Pulmonary lymphangiomyomatosis Achromatic retinal patches Sertoli cell neoplasm Renal cell carcinoma Rhabdomyoma Specific learning disability Cognitive impairment Behavioral abnormality Global developmental delay Seizures Intellectual disability Autism Intra-oral hyperpigmentation EEG abnormality Anxiety Abnormality of circulating adrenocorticotropin level Attention deficit hyperactivity disorder Papule Iris coloboma Thyroid follicular hyperplasia Cerebral calcification Hamartoma Generalized-onset seizure Bradycardia Aplasia/Hypoplasia of the corpus callosum Hypopigmented skin patches Increased intracranial pressure Atrioventricular block Precocious puberty Abnormality of neuronal migration Emphysema Prominent occiput Cortical dysplasia Macule Infantile spasms Multiple cafe-au-lait spots Subungual fibromas Subependymal giant-cell astrocytoma Abdominal aortic aneurysm Enlarged polycystic ovaries Thyroid adenoma Generalized hyperpigmentation Adrenocortical carcinoma Testicular neoplasm Increased serum iron Abnormality of iron homeostasis Abnormality of the anterior pituitary Elevated transferrin saturation Abnormality of endocrine pancreas physiology Pituitary prolactin cell adenoma Microcephaly Neoplasm of the breast Abnormal facial shape Severe short stature Retinal detachment Osteochondroma Ventricular hypertrophy Multiple lentigines Microretrognathia Schwannoma Metaphyseal widening Aortic aneurysm Cone-shaped epiphysis Glucose intolerance Glycosuria Slender long bone Red hair Elevated circulating follicle stimulating hormone level Elevated circulating luteinizing hormone level Acute pancreatitis Pancreatic adenocarcinoma Azoospermia Growth delay Histiocytoma Anemia Peripheral Schwannoma Profuse pigmented skin lesions Blue nevus Pneumonia Hepatocellular adenoma Pallor Pigmented micronodular adrenocortical disease Cardiac myxoma Abnormality of the cardiovascular system Microcytic anemia Hypochromic microcytic anemia Hypochromic anemia Atransferrinemia Bronchogenic cyst Hypogonadotrophic hypogonadism Uterine neoplasm Hypertension associated with pheochromocytoma Nodular goiter Vestibular Schwannoma Fibroadenoma of the breast Increased urinary cortisol level Abdominal pain Adrenal pheochromocytoma Dilated cardiomyopathy Lethargy Delayed puberty Pituitary growth hormone cell adenoma Abnormal prolactin level Recurrent paroxysmal headache Proximal upper limb muscle hypertrophy



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