Melanoma, and Hyperlipidemia

Diseases related with Melanoma and Hyperlipidemia

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

Top matches:

HYPERLIPIDEMIA, COMBINED, 1 Is also known as hyplip1|hyperlipidemia, familial combined, 1|fchl1

Related symptoms:

  • Hyperlipidemia
  • Abnormality of lipid metabolism


SOURCES: MESH OMIM MENDELIAN

More info about HYPERLIPIDEMIA, COMBINED, 1

Congenital analbuminemia (CAA) is characterized by the absence or dramatic reduction of circulating human serum albumin (HSA).

Related symptoms:

  • Neoplasm
  • Fatigue
  • Edema
  • Osteoporosis
  • Carcinoma


SOURCES: OMIM ORPHANET MENDELIAN

More info about CONGENITAL ANALBUMINEMIA

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

Palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome is characterised by sex reversal in males with a 46, XX (SRY-negative) karyotype, palmoplantar hyperkeratosis and a predisposition to squamous cell carcinoma. To date, five cases (four of whom were brothers) have been described. The aetiology is unknown.

PALMOPLANTAR KERATODERMA-XX SEX REVERSAL-PREDISPOSITION TO SQUAMOUS CELL CARCINOMA SYNDROME Is also known as palmoplantar hyperkeratosis-xx sex reversal-predisposition to squamous cell carcinoma syndrome

Related symptoms:

  • Hearing impairment
  • Strabismus
  • Hypospadias
  • Hyperkeratosis
  • Carcinoma


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about PALMOPLANTAR KERATODERMA-XX SEX REVERSAL-PREDISPOSITION TO SQUAMOUS CELL CARCINOMA SYNDROME

Muir-Torre syndrome (MTS) is a form of hereditary nonpolyposis colon cancer (HNPCC) characterized by cutaneous sebaceous tumors, keratoacanthomas and at least one visceral malignancy, most frequently gastrointestinal carcinoma.

MUIR-TORRE SYNDROME Is also known as cutaneous sebaceous neoplasms and keratoacanthomas, multiple, with gastrointestinal and other carcinomas|multiple keratoacanthoma, muir-torre type

Related symptoms:

  • Neoplasm
  • Carcinoma
  • Leukemia
  • Nevus
  • Lymphoma


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about MUIR-TORRE SYNDROME

Adult-onset type II citrullinemia is an autosomal recessive metabolic disorder characterized clinically by the sudden onset of various neuropsychologic symptoms such as disorientation, abnormal behavior, convulsions, and coma due to hyperammonemia. In some cases, rapid progression can lead to brain edema and death if liver transplantation is not possible. Some patients may present with nonalcoholic hepatic steatosis or may develop hepatic fibrosis or hepatocellular carcinoma. Patients with this disorder have a natural aversion to carbohydrates and favor protein, which is in contrast to protein aversion usually observed in patients with urea cycle defects (summary by Komatsu et al., 2008).

CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2 Is also known as citrin deficiency

Related symptoms:

  • Seizures
  • Tremor
  • Edema
  • Vomiting
  • Diarrhea


SOURCES: ORPHANET OMIM MENDELIAN

More info about CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2

GLYCOGEN STORAGE DISEASE IC; GSD1C Is also known as gsd ic

Related symptoms:

  • Hypertension
  • Hepatomegaly
  • Renal insufficiency
  • Hypoglycemia
  • Proteinuria


SOURCES: ORPHANET OMIM MENDELIAN

More info about GLYCOGEN STORAGE DISEASE IC; GSD1C

Acute intermittent porphyria is the most frequent and the most severe form of the acute hepatic porphyrias (see this term). It is characterized by the occurrence of neuro-visceral attacks without cutaneous manifestations.

ACUTE INTERMITTENT PORPHYRIA Is also known as ups deficiency|porphyria, swedish type|pbgd deficiency|porphobilinogen deaminase deficiency|uroporphyrinogen synthase deficiency

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Muscle weakness
  • Pain


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about ACUTE INTERMITTENT PORPHYRIA

Top 5 symptoms//phenotypes associated to Melanoma and Hyperlipidemia

Symptoms // Phenotype % cases
Carcinoma Uncommon - Between 30% and 50% cases
Neoplasm Uncommon - Between 30% and 50% cases
Hepatocellular carcinoma Uncommon - Between 30% and 50% cases
Laryngeal carcinoma Rare - less than 30% cases
Psychosis Rare - less than 30% cases

Other less frequent symptoms

Patients with Melanoma and Hyperlipidemia. may also develop some of the following symptoms:

Rare Symptoms - Less than 30% cases

Hypertension Hypertriglyceridemia Lethargy Delirium Coma Diarrhea Vomiting Renal insufficiency Insomnia Hallucinations Hypoalbuminemia Hypercholesterolemia Edema Seizures Xanthomatosis Gout Elevated urinary delta-aminolevulinic acid Hepatoblastoma Xanthelasma Decreased glomerular filtration rate Pulmonary arterial hypertension Chronic pancreatitis Spider hemangioma Ketonemia Intellectual disability Focal segmental glomerulosclerosis Proteinuria Metabolic acidosis Hematuria Lactic acidosis Delayed puberty Muscle weakness Hypoglycemia Hepatomegaly Hypoargininemia Delayed menarche Mania Cerebral edema Enuresis Echolalia Intrahepatic cholestasis Delusions Global developmental delay Intellectual disability, mild Pain Ileus Anorexia Paraparesis Cranial nerve paralysis Hyponatremia Apathy Agitation Dysuria Urinary retention Urinary incontinence Red urine Diaphragmatic paralysis Abnormal urinary color Psychotic episodes Hypertensive crisis Respiratory paralysis Paralytic ileus Cutaneous photosensitivity Abdominal distention Anemia Hepatosplenomegaly Behavioral abnormality Depressivity Constipation Hyperhidrosis Abdominal pain Weight loss Arthralgia Myalgia Nephropathy Anxiety Paralysis Nausea and vomiting Paresthesia Stage 5 chronic kidney disease Nausea Tachycardia Arrhythmia Cholestasis Drowsiness Ovotestis Palmoplantar hyperkeratosis Premature ovarian insufficiency Clitoral hypertrophy Squamous cell carcinoma Sex reversal Squamous cell carcinoma of the skin Palmoplantar hyperhidrosis Small nail Sclerodactyly Premature loss of permanent teeth Orthokeratotic hyperkeratosis Leukemia Nevus Lymphoma Vasculitis Gynecomastia Ambiguous genitalia Breast carcinoma Hypercoagulability Fatigue Osteoporosis Small for gestational age Hypotension Atherosclerosis Lipodystrophy Asthenia Decreased testicular size Hearing impairment Strabismus Hypospadias Hyperkeratosis Corneal opacity Nail dystrophy Palmoplantar keratoderma Neoplasm of the skin Basal cell carcinoma Restlessness Abnormality of the liver Tremor Obesity Hyperactivity Elevated hepatic transaminase Aggressive behavior Irritability Confusion Malignant genitourinary tract tumor Hepatic steatosis Memory impairment Abnormality of lipid metabolism Decreased liver function Hepatic fibrosis Pancreatitis Hyperammonemia Benign genitourinary tract neoplasm Benign gastrointestinal tract tumors Colon cancer Colonic diverticula Hodgkin lymphoma Renal neoplasm Neoplasm of the liver Intestinal polyposis Chondrosarcoma Adenoma sebaceum Intestinal polyp Salivary gland neoplasm Endometrial carcinoma Hereditary nonpolyposis colorectal carcinoma Hematological neoplasm Neoplasm of the stomach Sebaceous gland carcinoma Duodenal adenocarcinoma Keratoacanthoma Acute episodes of neuropathic symptoms


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