Melanoma, and Schizophrenia

Diseases related with Melanoma and Schizophrenia

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


Top matches:

Low match HYPERPROLINEMIA TYPE 1


Hyperprolinaemia type I is an inborn error of proline metabolism characterised by elevated levels of proline in the plasma and urine. The prevalence is unknown. The disorder is generally considered to be benign but associations with renal abnormalities, epileptic seizures, and other neurological manifestations, as well as certain forms of schizophrenia have been reported. It is transmitted as an autosomal recessive trait and is caused by mutations in the proline dehydrogenase or proline oxidase gene (PRODH or POX, 22q11.2).

HYPERPROLINEMIA TYPE 1 Is also known as hpi|proline oxidase deficiency

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Hearing impairment


SOURCES: OMIM ORPHANET MENDELIAN

More info about HYPERPROLINEMIA TYPE 1

Low match 15Q13.3 MICRODELETION SYNDROME


15q13.3 microdeletion (microdel15q13.3) syndrome is characterized by a wide spectrum of neurodevelopmental disorders with no or subtle dysmorphic features.

15Q13.3 MICRODELETION SYNDROME Is also known as del(15)(q13.3)|chromosome 15q13.3 microdeletion syndrome|monosomy 15q13.3

Related symptoms:

  • Seizures
  • Schizophrenia
  • Bipolar affective disorder


SOURCES: MESH MENDELIAN

More info about 15Q13.3 MICRODELETION SYNDROME

Low match WILSON DISEASE


Wilson disease is a very rare inherited multisystemic disease presenting non-specific neurological, hepatic, psychiatric or osseo-muscular manifestations due to excessive copper deposition in the body.

WILSON DISEASE Is also known as wd|hepatolenticular degeneration|wnd

Related symptoms:

  • Intellectual disability
  • Growth delay
  • Neoplasm
  • Failure to thrive
  • Spasticity


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about WILSON DISEASE

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Other less relevant matches:

Low match DRUG METABOLISM, POOR, CYP2D6-RELATED


Related symptoms:

  • Neoplasm
  • Hypertension
  • Abnormality of metabolism/homeostasis
  • Depressivity
  • Hypotension


SOURCES: MESH OMIM MENDELIAN

More info about DRUG METABOLISM, POOR, CYP2D6-RELATED

Low match MAJOR DEPRESSIVE DISORDER; MDD


MAJOR DEPRESSIVE DISORDER; MDD Is also known as unipolar depression

Related symptoms:

  • Neoplasm
  • Behavioral abnormality
  • Depressivity
  • Anxiety
  • Abnormality of the liver


SOURCES: OMIM MENDELIAN

More info about MAJOR DEPRESSIVE DISORDER; MDD

Low match SCHIZOPHRENIA 18; SCZD18


SCHIZOPHRENIA 18; SCZD18 Is also known as schizophrenia 18 with or without an affective disorder

Related symptoms:

  • Schizophrenia


SOURCES: OMIM MENDELIAN

More info about SCHIZOPHRENIA 18; SCZD18

Low match SCHIZOPHRENIA 4; SCZD4


SCHIZOPHRENIA 4; SCZD4 Is also known as schizophrenia susceptibility locus, chromosome 22q11-related

Related symptoms:

  • Abnormality of metabolism/homeostasis
  • Schizophrenia


SOURCES: OMIM MENDELIAN

More info about SCHIZOPHRENIA 4; SCZD4

Low match SCHIZOPHRENIA 19; SCZD19


SCHIZOPHRENIA 19; SCZD19 Is also known as schizophrenia 19 with or without an affective disorder

Related symptoms:

  • Behavioral abnormality
  • Psychosis
  • Schizophrenia
  • Bipolar affective disorder


SOURCES: OMIM MENDELIAN

More info about SCHIZOPHRENIA 19; SCZD19

Low match 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 malignant melanoma, see {155600}.

Related symptoms:

  • Neoplasm
  • Melanoma


SOURCES: OMIM MENDELIAN

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

Top 5 symptoms//phenotypes associated to Melanoma and Schizophrenia

Symptoms // Phenotype % cases
Neoplasm Uncommon - Between 30% and 50% cases
Behavioral abnormality Uncommon - Between 30% and 50% cases
Depressivity Uncommon - Between 30% and 50% cases
Bipolar affective disorder Uncommon - Between 30% and 50% cases
Intellectual disability Rare - less than 30% cases
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Other less frequent symptoms

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

Rare Symptoms - Less than 30% cases


Abnormality of metabolism/homeostasis Psychosis Seizures Abnormality of the liver Anxiety Proteinuria Aggressive behavior Leukoencephalopathy Abnormality of blood and blood-forming tissues Arthropathy Osteomalacia Glycosuria Pathologic fracture Global brain atrophy Oral-pharyngeal dysphagia Personality changes Abnormality of mitochondrial metabolism Hypercalciuria Back pain Abnormality of the hand Drooling Leukopenia Hepatocellular carcinoma Nephrocalcinosis Aminoaciduria Spontaneous abortion Muscle stiffness Increased body weight Bone pain Decreased liver function Nephrolithiasis Involuntary movements Clumsiness Cholestasis Osteoarthritis Progressive neurologic deterioration Joint swelling Hypoparathyroidism Hepatitis Hypersexuality Suicidal ideation Agoraphobia Mania Alcoholism Stroke Hypotension Global developmental delay Hypertension Atypical or prolonged hepatitis Kayser-Fleischer ring Mixed demyelinating and axonal polyneuropathy High nonceruloplasmin-bound serum copper Acute hepatitis Poor motor coordination Hand tremor Hypocupremia Premature osteoarthritis Abnormality of the menstrual cycle Retinoblastoma Proximal muscle weakness in lower limbs Menstrual irregularities Neoplasm of the liver Hyperphosphaturia Esophageal varix Chondrocalcinosis Acute hepatic failure Renal tubular dysfunction Increased reactive oxygen species production Generalized hypotonia Coma Ascites EEG abnormality Dystonia Vomiting Edema Dysphagia Fatigue Tremor Dysarthria Hepatomegaly Peripheral neuropathy Anemia Spasticity Failure to thrive Growth delay Hyperprolinemia Cerebral atrophy Prolinuria Hydroxyprolinuria Hyperglycinuria Motor deterioration Bruxism Nephroblastoma Nephritis Severe muscular hypotonia Stereotypy Hemiparesis Status epilepticus Sleep disturbance Nephropathy Splenomegaly Thrombocytopenia Ichthyosis Nausea and vomiting Polyneuropathy Hepatic steatosis Hemolytic anemia Bruising susceptibility Hepatic failure Hearing impairment Cirrhosis Nausea Peripheral axonal neuropathy Paresthesia Confusion Poor speech Infertility Abnormality of the cerebral white matter Hyperactivity Pruritus Muscular hypotonia Abnormality of the nervous system Delayed speech and language development Arthritis Elevated hepatic transaminase Rigidity Difficulty walking Hepatosplenomegaly Jaundice Arthralgia Weight loss Osteoporosis Dementia Joint hypermobility



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Microphthalmia and Hydronephrosis, related diseases and genetic alterations

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