ODCs

Cytoscape Web

Click node...

Huntington disease

1 OMIM reference -
1 associated gene
8 signs/symptoms

PROTEIN INTERACTIONS: 1
COMMON SIGNS: 1

Familial dysautonomia

1 OMIM reference -
1 associated gene
37 signs/symptoms

Huntington disease

Familial dysautonomia

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HTT	(0.8)	IKBKAP

Citations in the biomedical literature:

Huntington disease		Familial dysautonomia
	Synonym(s): - Huntington chorea		Synonym(s): - HSAN3 - Hereditary sensory and autonomic neuropathy type 3 - Riley-Day syndrome

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

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

	Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: variable Average age of death: any age 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: 1 OMIM reference - 1 MeSH reference: D006816		External references: 1 OMIM reference - 1 MeSH reference: D004402


COMMON SIGNS	- Psychic / behavioural troubles

Huntington disease		Familial dysautonomia
	Frequent - Abnormal cry / voice / phonation disorder / nasal speech - Autosomal dominant inheritance - Cortical atrophy without hydrocephaly / cerebral hemiatrophy / subcortical atrophy - EEG anomalies - Hypertonia / spasticity / rigidity / stiffness - Movement disorder - Psychic / psychomotor regression / dementia / intellectual decline		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 - 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