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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 1,741-1,760 of 10,888 diseases
MONDO:0013985
Autosomal recessive nonsyndromic hearing loss 18B is a genetic condition that primarily affects auditory function. It is caused by mutations in the OT...
MONDO:0009076
Autosomal recessive nonsyndromic hearing loss 1A is a congenital disorder affecting the auditory system, typically resulting in profound sensorineural...
MONDO:0012977
Autosomal recessive nonsyndromic hearing loss 1B is a condition that primarily affects the auditory system, leading to difficulties with hearing that...
MONDO:0010807
Autosomal recessive nonsyndromic hearing loss 2 (DFNB2) is caused by mutations in the MYO7A gene. This condition is characterized by hearing loss that...
MONDO:0011392
Autosomal recessive nonsyndromic hearing loss 20 (DFNB20) is a type of hearing loss characterized by its inheritance pattern, which is autosomal reces...
MONDO:0011351
Autosomal recessive nonsyndromic hearing loss 21 is caused by mutations in the TECTA gene. This condition is characterized by hearing loss that is not...
MONDO:0011762
Autosomal recessive nonsyndromic hearing loss 22 is a genetic condition caused by mutations in the OTOA gene. This condition is characterized by heari...
MONDO:0012293
Autosomal recessive nonsyndromic hearing loss 23 is a condition primarily affecting the auditory system, characterized by sensorineural hearing impair...
MONDO:0012602
Autosomal recessive nonsyndromic hearing loss 24 (DFNB24) is caused by mutations in the RDX gene. This condition is characterized by hearing loss that...
MONDO:0013210
Autosomal recessive nonsyndromic hearing loss 25 is a condition characterized primarily by hearing impairment and may include a gradual progression of...
MONDO:0011553
Autosomal recessive nonsyndromic hearing loss 26, also known as DFNB26, is caused by variations in the GAB1 gene located on chromosome 4q31. This cond...
MONDO:0011602
Autosomal recessive nonsyndromic hearing loss 27 (DFNB27) is characterized by hearing impairment due to variations in the chromosome region 2q23-q31....
MONDO:0012355
Autosomal recessive nonsyndromic hearing loss 28 is caused by mutations in the TRIOBP gene, which encodes a protein involved in actin binding and cell...
MONDO:0013537
Autosomal recessive nonsyndromic hearing loss 29 is caused by mutations in the CLDN14 gene. This condition leads to hearing loss that is not associate...
MONDO:0010860
Autosomal recessive nonsyndromic hearing loss 3 is caused by mutations in the MYO15A gene. This condition is inherited in an autosomal recessive manne...
MONDO:0011774
Autosomal recessive nonsyndromic hearing loss 30 is caused by mutations in the MYO3A gene. This condition is inherited in an autosomal recessive manne...
MONDO:0011767
Autosomal recessive nonsyndromic hearing loss 31 is a condition characterized primarily by sensorineural hearing impairment, which results from mutati...
MONDO:0012091
Autosomal recessive nonsyndromic hearing loss 32 is a form of inherited deafness that presents with prelingual, severe to profound, and stable hearing...
MONDO:0011799
Autosomal recessive nonsyndromic hearing loss 33, also known as DFNB33, is a form of deafness that arises from genetic variations in the chromosome re...
MONDO:0012060
Autosomal recessive nonsyndromic hearing loss 35 is a condition characterized by sensorineural hearing impairment due to mutations in the ESRRB gene....
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.