Disease Directory

Trusted information across 10,888 rare diseases — plain language, always cited, free for everyone.

Search by:Disease•Gene•Symptom•Treatment•PAG•OMIM/Orphanet ID

Commonly searched:Cystic Fibrosis Duchenne Huntington's ALS Sickle Cell

Can't find your disease? Try searching by gene, symptom, or OMIM ID.

Discover by:

Browse by category:

QC-Validated

Every report passes a 3-tier quality pipeline with gene validation, fact-checking, and safety checks.

10+ Authoritative Sources

Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and more. Every claim is cited.

Always Current

Data syncs range from 3x daily (news) to weekly (trials, FDA). Reports regenerate when data changes.

Showing 8,201-8,220 of 10,888 diseases

hearing loss, autosomal recessive 108

MONDO:0033200

Rare

ROR1

hearing loss, autosomal recessive 109

MONDO:0033202

Rare

ESRP1

hearing loss, autosomal recessive 110

MONDO:0054860

Rare

Hearing loss, autosomal recessive 110 is an inherited condition that primarily affects the auditory system, leading to sensorineural hearing impairmen...

COCH

hearing loss, autosomal recessive 111

MONDO:0029142

Rare

MPZL2

hearing loss, autosomal recessive 112

MONDO:0032639

Rare

Hearing loss, autosomal recessive 112 is a genetic condition primarily characterized by sensorineural hearing impairment. It is associated with varian...

BDP1

hearing loss, autosomal recessive 113

MONDO:0032732

Rare

CEACAM16

hearing loss, autosomal recessive 114

MONDO:0032761

Rare

GRAP

hearing loss, autosomal recessive 115

MONDO:0032762

Rare

Hearing loss, autosomal recessive 115 is an inherited condition that primarily affects the ear, resulting in sensorineural hearing impairment. This co...

SPNS2

hearing loss, autosomal recessive 116

MONDO:0033670

Rare

Hearing loss, autosomal recessive 116 is a genetic condition that primarily affects the auditory system, leading to sensorineural hearing impairment....

CLDN9

hearing loss, autosomal recessive 117

MONDO:0030905

Rare

Hearing loss, autosomal recessive 117 is a genetic condition primarily affecting auditory function, with sensorineural hearing impairment as its defin...

CLRN2

hearing loss, autosomal recessive 118, with cochlear aplasia

MONDO:0030449

Rare

Hearing loss, autosomal recessive 118, with cochlear aplasia is a condition that affects the auditory system, with affected individuals typically pres...

hearing loss, autosomal recessive 119

MONDO:0030480

Rare

AFG2B

hearing loss, autosomal recessive 120

MONDO:0859374

Rare

MINAR2

hearing loss, autosomal recessive 121

MONDO:0957825

Rare

GPR156

hearing loss, autosomal recessive 122

MONDO:0958228

Rare

TMTC4

hearing loss, autosomal recessive 123

MONDO:0958277

Rare

STX4

hearing loss, autosomal recessive 125

MONDO:0971152

Rare

GAS2

hearing loss, autosomal recessive 57

MONDO:0033201

Rare

Hearing loss, autosomal recessive 57 is a condition primarily affecting the auditory system, characterized by sensorineural hearing impairment. It is...

PDZD7

hearing loss, autosomal recessive 94

MONDO:0032749

Rare

NARS2

hearing loss, autosomal recessive 99

MONDO:0032776

Rare

TMEM132E

Previous411 / 545Next

Stay informed about your disease

Create a free account to follow diseases and receive weekly updates on clinical trials, FDA decisions, and research news. Free forever.

Already have an account? Sign in

Turn this intelligence into published content.

Organizations use Kisho to generate AI research reports, collaborate with their team, and publish directly to WordPress — all powered by the same data you see here.

Know something that's missing or incorrect? Suggest a Correction · Share Your Story