ODCs

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2 OMIM references -
2 associated genes
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

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

X-linked diffuse leiomyomatosis - Alport syndrome

X-linked nonsyndromic sensorineural deafness type DFN


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	COL4A5	(0.52)	COL4A6

Citations in the biomedical literature:

X-linked diffuse leiomyomatosis - Alport syndrome		X-linked nonsyndromic sensorineural deafness type DFN
	Synonym(s): - Xq22.3 microdeletion syndrome		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

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare renal disease		Classification (Orphanet): - Rare genetic disease - Rare otorhinolaryngologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the ear and mastoid process -

	Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: x-linked dominant		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: x-linked recessive

	External references: 2 OMIM references - No MeSH references		External references: 4 OMIM references - No MeSH references

No signs/symptoms info available.