Fever, and Basal cell carcinoma

Diseases related with Fever and Basal cell carcinoma

In the following list you will find some of the most common rare diseases related to Fever and Basal cell carcinoma that can help you solving undiagnosed cases.

Top matches:

Abetalipoproteinemia/ homozygous familial hypobetalipoproteinemia (ABL/HoFHBL) is a severe form of familial hypobetalipoproteinemia (see this term) characterized by permanently low levels (below the 5th percentile) of apolipoprotein B and LDL cholesterol, and by growth delay, malabsorption, hepatomegaly, and neurological and neuromuscular manifestations.

ABETALIPOPROTEINEMIA Is also known as hypobetalipoproteinemia, normotriglyceridemic|fhbl|hypobetalipoproteinemia, familial|acanthocytosis with hypobetalipoproteinemia|homozygous familial hypobetalipoproteinemia|bassen-kornzweig disease

Related symptoms:

  • Global developmental delay
  • Ataxia
  • Muscular hypotonia
  • Anemia
  • Visual impairment


SOURCES: ORPHANET OMIM MENDELIAN

More info about ABETALIPOPROTEINEMIA

Low match KAPOSI SARCOMA

Kaposi sarcoma (KS) is a rare human herpes virus 8 (HHV-8)-induced endothelial inflammatory neoplasm that develops is various clinically distinct settings, manifesting mostly as cutaneous lesions, or mucosal or visceral involvement.

KAPOSI SARCOMA Is also known as multiple idiopathic pigmented hemangiosarcoma, susceptibility to

Related symptoms:

  • Neoplasm
  • Hypertension
  • Fever
  • Fatigue
  • Edema


SOURCES: OMIM ORPHANET MENDELIAN

More info about KAPOSI SARCOMA

Sézary syndrome (SS) is an aggressive form of cutaneous T-cell lymphoma characterized by a triad of erythroderma, lymphadenopathy and circulating atypical lymphocytes (Sézary cells).

SÉZARY SYNDROME Is also known as sÉzary lymphoma

Related symptoms:

  • Neoplasm
  • Abnormal facial shape
  • Peripheral neuropathy
  • Hepatomegaly
  • Fever


SOURCES: MESH ORPHANET MENDELIAN

More info about SÉZARY SYNDROME

Other less relevant matches:

Low match NEUROBLASTOMA

Neuroblastoma is a malignant tumor of neural crest cells, the cells that give rise to the sympathetic nervous system, which is observed in children.

Related symptoms:

  • Ataxia
  • Neoplasm
  • Failure to thrive
  • Pain
  • Anemia


SOURCES: ORPHANET OMIM MENDELIAN

More info about NEUROBLASTOMA

Gastrointestinal stromal tumor (GIST) is the most common mesenchymal neoplasm of the gastrointestinal (GI) tract, typically presenting in adults over the age of 40 (mean age 63), and only rarely in children, in various regions of the GI tract, most commonly the stomach or small intestine but also less commonly in the esophagus, appendix, rectum and colon. GISTs can be asymptomatic or present with various non-specific signs, depending on the location and size of tumor, such as loss of appetite, anemia, weight loss, fatigue, abdominal discomfort or fullness, nausea, vomiting, as well as an abdominal mass, blood in stool, and intestinal obstruction. GISTs can also be seen in familial syndromes such as Carney triad and neurofibromatosis type 1.

GASTROINTESTINAL STROMAL TUMOR Is also known as gastrointestinal stromal sarcoma|gist

Related symptoms:

  • Neoplasm
  • Pain
  • Anemia
  • Fever
  • Fatigue


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about GASTROINTESTINAL STROMAL TUMOR

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 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

Agammaglobulinemia, non-Bruton type (autosomal agammaglobulinemia) is a rare form of agammaglobulinemia, a primary immunodeficiency disease, and is characterized by variable immune dysfunction with frequent and recurrent bacterial infections and/or chronic diarrhea.

AUTOSOMAL AGAMMAGLOBULINEMIA Is also known as agammaglobulinemia, autosomal recessive, due to ighm defect|agammaglobulinemia, non-bruton type

Related symptoms:

  • Hypertelorism
  • Failure to thrive
  • High palate
  • Epicanthus
  • Fever


SOURCES: OMIM ORPHANET MENDELIAN

More info about AUTOSOMAL AGAMMAGLOBULINEMIA

Netherton syndrome (NS) is a skin disorder characterized by congenital ichthyosiform erythroderma (CIE), a distinctive hair shaft defect (trichorrhexis invaginata; TI) and atopic manifestations.

NETHERTON SYNDROME Is also known as erythroderma, ichthyosiform, with hypotrichosis and hyper-ige|comÈl-netherton syndrome|bamboo hair syndrome|comel-netherton syndrome|ns|netherton disease

Related symptoms:

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


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about NETHERTON SYNDROME

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

Top 5 symptoms//phenotypes associated to Fever and Basal cell carcinoma

Symptoms // Phenotype % cases
Neoplasm Common - Between 50% and 80% cases
Weight loss Common - Between 50% and 80% cases
Skin rash Uncommon - Between 30% and 50% cases
Fatigue Uncommon - Between 30% and 50% cases
Immunodeficiency Uncommon - Between 30% and 50% cases

Other less frequent symptoms

Patients with Fever and Basal cell carcinoma. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases

Diarrhea Decreased antibody level in blood Paraganglioma Neurofibromas Pneumonia Congestive heart failure Lymphoma Pain Verrucae Hypertension Failure to thrive Irregular hyperpigmentation Malabsorption Abnormality of the liver Carcinoma Neoplasm of the skin Sarcoma Hypermelanotic macule Anemia

Rare Symptoms - Less than 30% cases

Abdominal pain Cafe-au-lait spot Erythroderma Dry skin Pruritus Neutropenia Dehydration Urticaria Cellulitis Arthritis Bronchiectasis Cardiac myxoma Sinusitis Meningitis Recurrent bacterial infections Osteomyelitis Growth hormone excess Heart murmur Schwannoma Ischemic stroke Ataxia Confusion Recurrent infections Seizures Recurrent respiratory infections Sepsis Skin nodule Recurrent skin infections Alopecia Global developmental delay Macule Gastrointestinal hemorrhage Lymphadenopathy Papule Peripheral neuropathy Hemangioma Chronic diarrhea Edema Myelokathexis Hypertelorism High palate Thyroid carcinoma Epicanthus Generalized hypopigmentation Pituitary adenoma Macroorchidism Hirsutism Cough Blue irides Increased circulating cortisol level Hepatitis Recurrent otitis media Recurrent pneumonia Conjunctivitis Bipolar affective disorder Encephalitis Chronic otitis media Bronchitis Striae distensae Recurrent sinusitis External ear malformation Bone marrow hypercellularity Tonsillitis Pheochromocytoma Pituitary prolactin cell adenoma Myxoid subcutaneous tumors Otitis media Recurrent urinary tract infections Thyroid follicular hyperplasia Profuse pigmented skin lesions Uterine leiomyoma Follicular thyroid carcinoma Recurrent upper respiratory tract infections Leukocytosis Combined immunodeficiency Follicular hyperplasia Testicular neoplasm IgG deficiency Hypersegmentation of neutrophil nuclei Periodontitis B-cell lymphoma Fibroma Multiple lentigines Atelectasis Abnormality of female internal genitalia Red hair Abnormality of female external genitalia Abnormality of bone marrow cell morphology Folliculitis Septic arthritis Freckling Agammaglobulinemia Intellectual disability B lymphocytopenia Immunologic hypersensitivity Severe postnatal growth retardation Hypothermia Villous atrophy Tall stature Allergy Congenital nonbullous ichthyosiform erythroderma Trichorrhexis nodosa Allergic rhinitis Palpitations Increased IgE level Angioedema Abnormality of the skin Congenital ichthyosiform erythroderma Hypernatremia Hypernatremic dehydration Brittle scalp hair IgE-mediated food allergy Muscle weakness Respiratory distress Osteoporosis Dyspnea Proximal muscle weakness Myalgia Nevus Abnormality of the eye Atopic dermatitis Abnormality of the musculature Crohn's disease Sparse and thin eyebrow Recurrent enteroviral infections Stroke Short stature Growth delay Hydronephrosis Ichthyosis Asthma Eczema Fine hair Sparse scalp hair Inflammatory abnormality of the skin Abnormality of the hair Gynecomastia Aminoaciduria Sparse eyelashes Acanthosis nigricans Abnormal intestine morphology Brittle hair Intracranial hemorrhage Scaling skin Precocious puberty Psoriasiform dermatitis Emphysema Malnutrition Increased body weight Ectopic kidney Cardiomegaly Carious teeth Abnormality of the face Generalized lymphadenopathy Skin plaque Susceptibility to herpesvirus Neoplasm by anatomical site Abnormal facial shape Hepatomegaly Skeletal muscle atrophy Tremor Splenomegaly Hepatosplenomegaly Nail dystrophy Hypotrichosis Palmoplantar keratoderma Thickened skin Cellular immunodeficiency Ectropion Gangrene Abnormality of the pleura Lichenification T-cell lymphoma Abnormal lymphocyte morphology Abnormal immunoglobulin level Cutaneous T-cell lymphoma Myoclonus Bone pain Abnormality of the thorax Neuroblastoma Spinal cord compression Venous insufficiency Abnormality of the spleen Neoplasm of the nervous system Renal cell carcinoma Muscular hypotonia Visual impairment Gait disturbance Thrombocytopenia Rod-cone dystrophy Abnormality of movement Retinal degeneration Hepatic failure Hepatic steatosis Peripheral demyelination Abnormality of retinal pigmentation Reduced tendon reflexes Abnormality of the coagulation cascade Acanthocytosis Lymphoproliferative disorder Fat malabsorption Hypocholesterolemia Decreased LDL cholesterol concentration Abetalipoproteinemia Increased HDL cholesterol concentration Steatocystoma multiplex Encephalopathy Pulmonary arterial hypertension Abnormal lung morphology Lymphedema Abnormal retinal morphology Abnormality of the gastrointestinal tract Abnormality of the lower limb Ganglioneuroma Horner syndrome Respiratory tract infection Tricuspid regurgitation Atrial septal defect Behavioral abnormality Headache Dilatation Jaundice Abnormality of skin pigmentation Coma Ascites Chest pain Syncope Mitral valve prolapse Cholestasis Easy fatigability Cerebral hemorrhage Giant hypertrophic gastritis Exertional dyspnea Thromboembolism Dilatation of the cerebral artery Subarachnoid hemorrhage Edema of the lower limbs Pulmonary edema Endocarditis Orthopnea Increased inflammatory response Bacterial endocarditis Pulmonic valve myxoma Hearing impairment Respiratory failure Cognitive impairment Neoplasm of the gastrointestinal tract Ganglioneuroblastoma Abdominal distention Adrenal calcification Opsoclonus Abdominal mass Elevated urinary dopamine Elevated urinary catecholamines Elevated urinary homovanillic acid Elevated urinary vanillylmandelic acid Dysphagia Vomiting Constipation Coarse facial features Pallor Nausea and vomiting Hyperpigmentation of the skin Gastrointestinal obstruction Eosinophilia Intestinal obstruction Large hands Lipoma Gastrointestinal stroma tumor Leiomyosarcoma Soft tissue sarcoma Mastocytosis Neoplasm of the small intestine Neoplasm of the rectum Esophageal neoplasm Neoplasm of the colon Neoplasm of the stomach Cutaneous myxoma


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