Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
Plain-language summaries of 10,888 rare conditions, drawn from MONDO, GeneReviews, ClinVar, FDA, NIH, ClinicalTrials.gov, PubMed, and 5 other public sources. Free, sourced, never gated.
Kisho provides public health information only — not medical advice. Always consult your healthcare provider.
12
authoritative sources — clinical, regulatory, scientific
10,888
rare conditions, continuously monitored
Daily
updates from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet…
Showing 6,661-6,680 of 10,888 diseases
MONDO:0019588
Hearing loss, autosomal recessive is a form of nonsyndromic deafness that primarily affects the auditory system. It results from genetic variants in a...
MONDO:0032740
Hearing loss, autosomal recessive 100 is characterized by sensorineural hearing impairment, which is the core clinical feature of this condition. It i...
MONDO:0033198
MONDO:0033199
MONDO:0033200
MONDO:0033202
MONDO:0054860
Hearing loss, autosomal recessive 110 is an inherited condition that primarily affects the auditory system, leading to sensorineural hearing impairmen...
MONDO:0029142
MONDO:0032639
Hearing loss, autosomal recessive 112 is a genetic condition primarily characterized by sensorineural hearing impairment. It is associated with varian...
MONDO:0032732
MONDO:0032761
MONDO:0032762
Hearing loss, autosomal recessive 115 is an inherited condition that primarily affects the ear, resulting in sensorineural hearing impairment. This co...
MONDO:0033670
Hearing loss, autosomal recessive 116 is a genetic condition that primarily affects the auditory system, leading to sensorineural hearing impairment....
MONDO:0030905
Hearing loss, autosomal recessive 117 is a genetic condition primarily affecting auditory function, with sensorineural hearing impairment as its defin...
MONDO:0030449
Hearing loss, autosomal recessive 118, with cochlear aplasia is a condition that affects the auditory system, with affected individuals typically pres...
MONDO:0030480
MONDO:0859374
MONDO:0957825
MONDO:0958228
MONDO:0958277
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.