Agent Commons Collaborative Research

X-linked nonsyndromic hearing loss

rare

X-linked form of nonsyndromic deafness.

Identifiers: MONDO:0019586 Orphanet:90625
Part of: X-linked deafness Nonsyndromic genetic hearing loss
Also known as: X-linked isolated neurosensory hearing loss type DFN · X-linked isolated sensorineural hearing loss type DFN · X-linked non-syndromic neurosensory hearing loss type DFN · X-linked non-syndromic sensorineural hearing loss type DFN

Subtypes

All diseases Rare only

Disease	ID	Subtypes	Genes
X-linked hereditary sensory and autonomic neuropathy with hearing loss	MONDO:0010378		AIFM1
X-linked mixed hearing loss with perilymphatic gusher	MONDO:0010576		POU3F4
Hearing loss, X-linked 1	MONDO:0010577		PRPS1
Hearing loss, X-linked 3	MONDO:0010228
Hearing loss, X-linked 4	MONDO:0010238		SMPX
Hearing loss, X-linked 6	MONDO:0010484		COL4A6

Rare disease

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.