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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 1,541-1,560 of 10,888 diseases
MONDO:0011568
Autosomal dominant nonsyndromic hearing loss 25 is a condition that primarily affects the auditory system, resulting in sensorineural hearing impairme...
MONDO:0012902
Autosomal dominant nonsyndromic hearing loss 27 (DFNA27) is caused by variations in the REST gene located on chromosome 4q12-q13.1. This condition is...
MONDO:0012083
Autosomal dominant nonsyndromic hearing loss 28 (DFNA28) is caused by mutations in the GRHL2 gene. This condition is inherited in an autosomal dominan...
MONDO:0010817
Autosomal dominant nonsyndromic hearing loss 2A is caused by mutations in the KCNQ4 gene. This genetic condition leads to hearing loss that is not ass...
MONDO:0012976
Autosomal dominant nonsyndromic hearing loss 2B (DFNA2B) is caused by mutations in the GJB3 gene, which encodes a gap junction protein crucial for inn...
MONDO:0011673
Autosomal dominant nonsyndromic hearing loss 30 (DFNA30) is characterized by its inheritance pattern, which follows an autosomal dominant model. This...
MONDO:0012086
Autosomal dominant nonsyndromic hearing loss 31 (DFNA31) is characterized by hearing impairment that is inherited in an autosomal dominant pattern. Th...
MONDO:0013632
Autosomal dominant nonsyndromic hearing loss 33 (DFNA33) is characterized by hearing loss that is inherited in an autosomal dominant manner. The preci...
MONDO:0011708
Autosomal dominant nonsyndromic hearing loss 36, also known as DFNA36, is caused by mutations in the TMC1 gene. This condition is inherited in an auto...
MONDO:0011103
Autosomal dominant nonsyndromic hearing loss 3A is caused by mutations in the GJB2 gene, which is critical for the formation of gap junctions in the i...
MONDO:0012975
Autosomal dominant nonsyndromic hearing loss 3B (DFNA3B) is caused by mutations in the GJB6 gene. This condition is characterized by hearing loss that...
MONDO:0014603
Autosomal dominant nonsyndromic hearing loss 40 is a condition characterized primarily by sensorineural hearing impairment. It is caused by mutations...
MONDO:0011994
Autosomal dominant nonsyndromic hearing loss 41 is caused by mutations in the P2RX2 gene. This condition is characterized by hearing loss that is not...
MONDO:0012030
Autosomal dominant nonsyndromic hearing loss 43 (DFNA43) is characterized by hearing impairment that is inherited in an autosomal dominant manner. Thi...
MONDO:0011832
Autosomal dominant nonsyndromic hearing loss 44 is a condition characterized primarily by sensorineural hearing impairment resulting from a mutation i...
MONDO:0012090
Autosomal dominant nonsyndromic hearing loss 47, also known as DFNA47, is characterized by hearing loss that is inherited in an autosomal dominant man...
MONDO:0011920
autosomal dominant nonsyndromic hearing loss 48 is an extremely rare condition. Because few cases have been documented, detailed clinical information...
MONDO:0012023
Autosomal dominant nonsyndromic hearing loss 49 (DFNA49) is characterized by moderate loss of hearing for low and mid frequencies and mild loss for hi...
MONDO:0010915
Autosomal dominant nonsyndromic hearing loss 4A is caused by mutations in the MYH14 gene. This genetic condition leads to hearing loss that is not ass...
MONDO:0013823
Autosomal dominant nonsyndromic hearing loss 4B is a condition that predominantly affects the auditory system, leading to sensorineural hearing impair...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.