ODCs

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4 OMIM references -
4 associated genes
9 signs/symptoms

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Familial or sporadic hemiplegic migraine

Duchenne muscular dystrophy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CACNA1A	(0.68)	LTBP4

Citations in the biomedical literature:

Familial or sporadic hemiplegic migraine		Duchenne muscular dystrophy
	Synonym(s): (no synonyms)		Synonym(s): - DMD - Severe dystrophinopathy, Duchenne type

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

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

	Epidemiological data: Class of prevalence: 1-5 / 10 000 Average age onset: childhood Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 100 000 Average age onset: childhood Average age of death: young adult Type of inheritance: x-linked recessive

	External references: 4 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D020388

Familial or sporadic hemiplegic migraine
	Very frequent - Autosomal dominant inheritance - Hemiplegia / diplegia / hemiparesia / limb palsy - Movement disorder Frequent - Ataxia / incoordination / trouble of the equilibrium - Nystagmus Occasional - EEG anomalies - Retinitis pigmentosa / retinal pigmentary changes - Sensorineural deafness / hearing loss - Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia
Duchenne muscular dystrophy
(no data available)