ODCs

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4 OMIM references -
3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
3 signs/symptoms

X-linked nonsyndromic sensorineural deafness type DFN

Hereditary cerebral hemorrhage with amyloidosis, Arctic type


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	COL4A6	(0.7)	APP

Citations in the biomedical literature:

X-linked nonsyndromic sensorineural deafness type DFN		Hereditary cerebral hemorrhage with amyloidosis, Arctic type
	Synonym(s): - X-linked isolated neurosensory deafness type DFN - X-linked isolated neurosensory hearing loss type DFN - X-linked isolated sensorineural deafness type DFN - X-linked isolated sensorineural hearing loss type DFN - X-linked nonsyndromic neurosensory deafness type DFN - X-linked nonsyndromic neurosensory hearing loss type DFN - X-linked nonsyndromic sensorineural hearing loss type DFN		Synonym(s): - HCHWA, Arctic type

	Classification (Orphanet): - Rare genetic disease - Rare otorhinolaryngologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease - Rare systemic or rheumatologic disease

	Classification (ICD10): - Diseases of the ear and mastoid process -		Classification (ICD10): (no data available)

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: x-linked recessive		Epidemiological data: (no data available)

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

Hereditary cerebral hemorrhage with amyloidosis, Arctic type
	Very frequent - Autosomal dominant inheritance - Psychic / behavioural troubles - Psychic / psychomotor regression / dementia / intellectual decline
X-linked nonsyndromic sensorineural deafness type DFN
(no data available)