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Familial melanoma

8 OMIM references -
6 associated genes
12 signs/symptoms

PROTEIN INTERACTIONS: 1

Familial dysautonomia

1 OMIM reference -
1 associated gene
37 signs/symptoms

Familial melanoma

Familial dysautonomia

CDK4	(UniProt - OMIM)		IKBKAP	(UniProt - OMIM)
CDKN2A	(UniProt - OMIM)
CDKN2B	(UniProt - OMIM)
CDKN2D	(UniProt - OMIM)
MC1R	(UniProt - OMIM)
TERT	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CDKN2B	(0.63)	IKBKAP

Citations in the biomedical literature:

Familial melanoma		Familial dysautonomia
	Synonym(s): (no synonyms)		Synonym(s): - HSAN3 - Hereditary sensory and autonomic neuropathy type 3 - Riley-Day syndrome

	Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare oncologic disease - Rare skin disease		Classification (Orphanet): - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare skin disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: 8 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D004402

Familial melanoma		Familial dysautonomia
	Very frequent - Capillary hemangioma / nevus / naevus flammeus / port-wine stain - Melanoma Frequent - Anomalies of the lymphatic system - Dry / squaly skin / exfoliation - Excessive freckling - Hair and scalp anomalies Occasional - Autosomal dominant inheritance - Breast neoplasm / tumor / carcinoma / cancer - Estomach / gastric neoplasm / tumor / carcinoma / cancer - Extrapyramidal syndrome - Pancreatic / pancreas neoplasm / tumor / carcinoma / cancer - Retinopathy		Very frequent - Abnormal EMG / electromyogram / electropmyography - Anomalies of eyelids, eyelashes and lacrimal system - Areflexia / hyporeflexia - Autosomal recessive inheritance - Failure to thrive / difficulties for feeding in infancy / growth delay - Hyperhidrosis / increased sweating - Hypohidrosis / decreased sweating / thermoregulation disorder / heat intolerance - Hypotension - Insensitivity to pain - Malignant hyperthermia - Peripheral neuropathy - Pupillary anomalies / mydriasis / myosis / tonic pupil Frequent - Abnormal gait - Ataxia / incoordination / trouble of the equilibrium - Chronic arterial hypertension - Corneal ulceration / perforation - Hypotonia - Psychic / behavioural troubles - Repeat respiratory infections - Scoliosis Occasional - Abnormal pleura / hydrothorax / pleuresia / pleural effusion / chylothorax - Acrocyanosis / Raynaud's phenomenon / vasomotor disorders - Cardiac rhythm disorder / arrhythmia - Corneal clouding / opacity / vascularisation - Gastroesophageal reflux / pyrosis / esophagitis / hiatal hernia / gastroparesia - Heterochromia / mixed colouring of iris - Hyponatremia - Mutiple fractures / bone fragility - Myopia - Optic nerve anomaly / optic atrophy / anomaly of the papilla - Osteolysis / osteoclasia / bone destruction / erosions - Osteonecrosis / bone infarction - Renal failure - Renal glomerular defect / glomerulopathy - Renal / kidney anomalies - Seizures / epilepsy / absences / spasms / status epilepticus - Structural anomaly of the peritoneum