Congestive heart failure, and Melanoma

Diseases related with Congestive heart failure and Melanoma

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

Top matches:

Low match WERNER SYNDROME

Werner syndrome (WS) is a rare inherited syndrome characterized by premature aging with onset in the third decade of life and with cardinal clinical features including bilateral cataracts, short stature, graying and thinning of scalp hair, characteristic skin disorders and premature onset of additional age-related disorders.

WERNER SYNDROME Is also known as ws|adult progeria

Related symptoms:

  • Short stature
  • Neoplasm
  • Pain
  • Cataract
  • Visual impairment


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about WERNER SYNDROME

Roberts syndrome (RBS) is characterized by pre- and postnatal growth retardation, severe symmetric limb reduction defects, craniofacial anomalies and severe intellectual deficit. SC phocomelia is a milder form of RBS.

ROBERTS SYNDROME Is also known as pseudothalidomide syndrome|roberts-sc phocomelia syndrome|sc pseudothalidomide syndrome|sc phocomelia

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Microcephaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about ROBERTS SYNDROME

Other less relevant matches:

Malignant melanoma is a neoplasm of pigment-producing cells called melanocytes that occurs most often in the skin, but may also occur in the eyes, ears, gastrointestinal tract, leptomeninges, and oral and genital mucous membranes (summary by Habif, 2010).For a discussion of genetic heterogeneity of malignant melanoma, see {155600}.

Related symptoms:

  • Neoplasm
  • Melanoma


SOURCES: OMIM MENDELIAN

More info about MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 5; CMM5

Malignant melanoma is a neoplasm of pigment-producing cells called melanocytes that occurs most often in the skin, but may also occur in the eyes, ears, gastrointestinal tract, leptomeninges, and oral and genital mucous membranes (summary by Habif, 2010).For a discussion of genetic heterogeneity of cutaneous malignant melanoma, see {155600}.

Related symptoms:

  • Neoplasm
  • Melanoma


SOURCES: OMIM MENDELIAN

More info about MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 6; CMM6

Familial glucocorticoid deficiency-5 is characterized by resistance to adrenocorticotropic hormone (ACTH) and isolated glucocorticoid deficiency, with typical biochemical findings of low serum cortisol levels and high plasma ACTH. Patients commonly present with hyperpigmentation (Prasad et al., 2014).For a discussion of genetic heterogeneity of familial glucocorticoid deficiency, see GCCD1 (OMIM ).

Related symptoms:

  • Ventricular septal defect
  • Congestive heart failure
  • Truncus arteriosus


SOURCES: OMIM MENDELIAN

More info about GLUCOCORTICOID DEFICIENCY 5; GCCD5

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

Segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome is a rare, genetic, polymalformative syndrome characterized by progressive, proportionate, asymmetric segmental overgrowth (with soft tissue hypertrophy and ballooning effect) that develops and progresses rapidly in early childhood, arteriovenous and lymphatic vascular malformations, lipomatosis and linear epidermal nevus (arranged in whorls along the lines of Blaschko). Clinical symptoms of Cowden syndrome, such as macrocephaly and progressive development of numerous hypertrophic hamartomatous and neoplastic lesions involving multiple organs and systems, are also associated. Patients present an increased risk of developing cancer.

SEGMENTAL OUTGROWTH-LIPOMATOSIS-ARTERIOVENOUS MALFORMATION-EPIDERMAL NEVUS SYNDROME Is also known as solamen syndrome

Related symptoms:

  • Macrocephaly
  • Congestive heart failure
  • Papule
  • Talipes
  • Recurrent fractures


SOURCES: ORPHANET MENDELIAN

More info about SEGMENTAL OUTGROWTH-LIPOMATOSIS-ARTERIOVENOUS MALFORMATION-EPIDERMAL NEVUS SYNDROME

Idiopathic pulmonary fibrosis (IPF) is a nonneoplastic pulmonary disease that is characterized by the formation of scar tissue within the lungs in the absence of any known cause.

IDIOPATHIC PULMONARY FIBROSIS Is also known as cfa|uip|usual interstitial pneumonia|interstitial pneumonitis, usual|idiopathic pulmonary fibrosis, familial|cryptogenic fibrosing alveolitis|fibrosing alveolitis, cryptogenic|fibrocystic pulmonary dysplasia

Related symptoms:

  • Neoplasm
  • Hypertension
  • Fever
  • Respiratory insufficiency
  • Respiratory distress


SOURCES: OMIM ORPHANET MENDELIAN

More info about IDIOPATHIC PULMONARY FIBROSIS

Low match WHIM SYNDROME

WHIM (warts, hypogammaglobulinemia, infections, and myelokathexis) syndrome is a congenital autosomal dominant immune deficiency characterized by abnormal retention of mature neutrophils in the bone marrow (myelokathexis) and occasional hypogammaglobulinemia, associated with an increased risk for bacterial infections and a susceptibility to human papillomavirus (HPV) induced lesions (cutaneous warts, genital dysplasia and invasive mucosal carcinoma).

WHIM SYNDROME Is also known as warts, hypogammaglobulinemia, infections, and myelokathexis syndrome|warts-infections-leukopenia-myelokatexis syndrome|wilm|warts-hypogammaglobulinemia-infections-myelokathexis syndrome

Related symptoms:

  • Hearing impairment
  • Neoplasm
  • Fever
  • Congestive heart failure
  • Immunodeficiency


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about WHIM SYNDROME

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

Symptoms // Phenotype % cases
Neoplasm Common - Between 50% and 80% cases
Carcinoma Uncommon - Between 30% and 50% cases
Pain Uncommon - Between 30% and 50% cases
Hypertension Uncommon - Between 30% and 50% cases
Short stature Rare - less than 30% cases

Other less frequent symptoms

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

Rare Symptoms - Less than 30% cases

Proptosis Bronchiectasis Myocardial infarction Chest pain Respiratory tract infection Pneumonia Ovarian neoplasm Respiratory failure Fever Cataract Pheochromocytoma Ventricular septal defect Truncus arteriosus Headache Hyperhidrosis Anxiety Tachycardia Palpitations Cranial nerve paralysis Neuroblastoma Renal cell carcinoma Recurrent fractures Paraganglioma Chemodectoma Gastrointestinal stroma tumor Talipes Recurrent paroxysmal headache Pulsatile tinnitus Papule Episodic paroxysmal anxiety Adrenal pheochromocytoma Macrocephaly Elevated urinary catecholamines Paraganglioma of head and neck Glomus jugular tumor Extraadrenal pheochromocytoma Hypertension associated with pheochromocytoma Premature separation of centromeric heterochromatin Facial hemangioma Midface capillary hemangioma Short femoral neck Synostosis of carpal bones Underdeveloped supraorbital ridges Absent radius Hip contracture Aplasia/Hypoplasia of the thumb Absent thumb Radial deviation of finger Severe intrauterine growth retardation Proximal placement of thumb Clitoral hypertrophy Radioulnar synostosis Polycystic kidney dysplasia Hypoplasia of the radius Hemangioma Sandal gap External ear malformation Upper limb undergrowth Tetraphocomelia Wrist flexion contracture Mesomelic arm shortening Progressive flexion contractures Absent earlobe Reduced bone mineral density Complete duplication of thumb phalanx Aplasia of the ulna Humeroradial synostosis Capillary hemangioma Phocomelia Long penis Subvalvular aortic stenosis Patellar aplasia Abnormality of the upper limb Fair hair Low hanging columella Subcutaneous nodule Lymphangioma Hemiplegia/hemiparesis Leukocytosis Ground-glass opacification on pulmonary HRCT Hearing impairment Immunodeficiency Arthritis Carious teeth Neutropenia Lymphoma Decreased antibody level in blood Otitis media Recurrent urinary tract infections Sinusitis Meningitis Recurrent bacterial infections Recurrent upper respiratory tract infections Combined immunodeficiency Reticular pattern on pulmonary HRCT Abnormality of female external genitalia Bone marrow hypercellularity Hypersegmentation of neutrophil nuclei Tonsillitis Septic arthritis Folliculitis Abnormality of bone marrow cell morphology Abnormality of female internal genitalia Osteomyelitis Atelectasis Verrucae B-cell lymphoma Periodontitis IgG deficiency Cellulitis Honeycomb lung Hypocapnia Hamartoma Cough Arteriovenous malformation Lower limb asymmetry Venous insufficiency Visceral angiomatosis Excessive wrinkled skin Neoplasm of the breast Wormian bones Upper limb asymmetry Neoplasm of the thyroid gland Respiratory insufficiency Respiratory distress Dyspnea Gastroesophageal reflux Scarring Cirrhosis Alveolar cell carcinoma Exertional dyspnea Crackles Pulmonary insufficiency Right ventricular failure Clubbing of fingers Pulmonary infiltrates Polycythemia Interstitial pulmonary abnormality Cyanosis Increased antibody level in blood Pulmonary fibrosis Clubbing Scaling skin Abnormal lung morphology Pulmonary arterial hypertension Opacification of the corneal stroma Hemiparesis Knee flexion contracture Premature graying of hair Atherosclerosis Breast carcinoma Laryngomalacia Sarcoma Dermal atrophy Lipodystrophy Abnormality of the voice Myelodysplasia Polydipsia Abnormality of the thorax Rocker bottom foot Polyuria Squamous cell carcinoma High pitched voice Polyphagia Type I diabetes mellitus Subcapsular cataract Progeroid facial appearance Posterior subcapsular cataract Pulmonary artery stenosis Neoplasm of the lung Alopecia of scalp Premature loss of teeth Prematurely aged appearance Decreased fertility Secondary amenorrhea Myeloid leukemia Scleroderma Telangiectasia of the skin Aplasia/Hypoplasia of the skin Lipoatrophy Macular degeneration Spontaneous abortion Renal neoplasm Osteoporosis Retinopathy Joint stiffness Micropenis Hyperkeratosis Diabetes mellitus Hypogonadism Rod-cone dystrophy Retinal degeneration Alopecia Behavioral abnormality Abnormality of the dentition Skeletal muscle atrophy Peripheral neuropathy Visual impairment Leukemia Nephropathy Hypergonadotropic hypogonadism Abnormality of retinal pigmentation Hoarse voice Increased bone mineral density Narrow face Abnormality of the hair Skin ulcer Insulin resistance Decreased body weight Small hand Sparse scalp hair Type II diabetes mellitus Decreased testicular size Convex nasal ridge Coma Hypopigmentation of the skin Meningioma Osteosarcoma Bilateral single transverse palmar creases Abnormality of cardiovascular system morphology Glaucoma Brachycephaly Posteriorly rotated ears Clinodactyly of the 5th finger Clinodactyly Thrombocytopenia Dilatation Retrognathia Microphthalmia Malar flattening Intellectual disability, mild Short neck Downslanted palpebral fissures Intrauterine growth retardation Polyhydramnios Postnatal growth retardation High palate Falls Aortic valve stenosis Short thumb Bowing of the long bones Blue sclerae Underdeveloped nasal alae Premature birth Cleft upper lip Paralysis Hypotrichosis Finger syndactyly Corneal opacity Prominent nasal bridge Sparse hair Craniosynostosis Brachydactyly Flexion contracture Abnormality of the cerebral vasculature Thyroid carcinoma Soft tissue sarcoma Chorioretinitis Cutaneous melanoma Narrow nasal ridge Arteriosclerosis Enlarged joints White forelock Poliosis Slender build Abnormality of the testis Pili torti Chondrocalcinosis Lack of skin elasticity Peripheral arterial stenosis Abnormal hair whorl Subcutaneous calcification Cryptorchidism Global developmental delay Cleft palate Micrognathia Nystagmus Hypertelorism Growth delay Microcephaly Seizures Neoplasm of the small intestine Intellectual disability Acral lentiginous melanoma Aplasia/Hypoplasia of the testes Neoplasm of the oral cavity Premature arteriosclerosis Gastrointestinal carcinoma Myelokathexis


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