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Rare Disease Intelligence — 10,888 conditions monitored | Kisho | Kisho

Open data · 12 authoritative sources

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What’s known, in plain language.

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.

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12

authoritative sources — clinical, regulatory, scientific

10,888

rare conditions, continuously monitored

Daily

updates from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet…

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Showing 1,201-1,220 of 10,888 diseases

arthrogryposis, distal, IIa 11

MONDO:0031045

Arthrogryposis, distal, IIa 11 is associated with variants in the MET gene and follows an autosomal dominant inheritance pattern. The clinical feature...

arthrogryposis, distal, type 12

MONDO:0957819

Arthrogryposis, distal, type 12 is an inherited condition primarily affecting the joints of the hands and feet, leading to congenital contractures and...

arthrogryposis, distal, type 1A

MONDO:0007157

Arthrogryposis, distal, type 1A is a condition affecting the musculoskeletal system that primarily involves joint contractures in the distal parts of...

arthrogryposis, distal, type 1B

MONDO:0013698

Arthrogryposis, distal, type 1B is a condition marked by congenital joint contractures that primarily affect the hands and feet. It falls within the s...

arthrogryposis, distal, type 1C

MONDO:0030847

Arthrogryposis, distal, type 1C is a congenital condition characterized primarily by joint contractures that affect the distal parts of the limbs, inc...

arthrogryposis, distal, type 2B2

MONDO:0032750

Arthrogryposis, distal, type 2B2 (DA2B2) is characterized by congenital joint contractures, specifically talipes equinovarus, which is present in all...

arthrogryposis, distal, type 2B3

MONDO:0032751

Arthrogryposis, distal, type 2B3 is a condition that primarily affects the musculoskeletal system, leading to joint contractures and alterations in li...

arthrogryposis, distal, type 2B4

MONDO:0800200

arthrogryposis, distal, type 2B4 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

arthrogryposis, distal, type 2E

MONDO:0007364

arthrogryposis, distal, type 2E is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

arthrogryposis, distal, with impaired proprioception and touch

MONDO:0014941

Arthrogryposis, distal, with impaired proprioception and touch is a condition primarily affecting the muscles and joints, with a significant impact on...

arthrogryposis due to muscular dystrophy

MONDO:0009679

Arthrogryposis due to muscular dystrophy is an extremely rare condition. Because few cases have been documented, detailed clinical information is limi...

arthrogryposis-ectodermal dysplasia-other anomalies syndrome

MONDO:0044406

Arthrogryposis-ectodermal dysplasia-other anomalies syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical...

arthrogryposis-hyperkeratosis syndrome, lethal form

MONDO:0008826

Arthrogryposis-hyperkeratosis syndrome, lethal form is an extremely rare condition. Because few cases have been documented, detailed clinical informat...

arthrogryposis-like hand anomaly-sensorineural deafness syndrome

MONDO:0007159

Arthrogryposis-like hand anomaly-sensorineural deafness syndrome is characterized by atypical hand development that resembles arthrogryposis and senso...

arthrogryposis-like syndrome

MONDO:0015241

Arthrogryposis-like syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

arthrogryposis multiplex congenita

MONDO:0015168

Arthrogryposis multiplex congenita (AMC) is a group of disorders characterized by congenital joint contractures that limit the range of motion in the...

KIF14UBA1GLE1+7

arthrogryposis multiplex congenita 1, neurogenic, with myelin defect

MONDO:0060486

Arthrogryposis multiplex congenita 1, neurogenic, with myelin defect is a complex condition that affects multiple body systems from birth, leading to...

arthrogryposis multiplex congenita 2, neurogenic type

MONDO:0008823

Arthrogryposis multiplex congenita 2, neurogenic type, is characterized by congenital immobility of the limbs, fixation of multiple joints, and muscle...

arthrogryposis multiplex congenita 3, myogenic type

MONDO:0032778

Arthrogryposis multiplex congenita 3, myogenic type is a congenital condition primarily affecting the muscles and joints, leading to multiple joint co...

arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum

MONDO:0032903

Arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum is a complex condition that primarily affects the musculoskelet...

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Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.