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

Open data · 12 authoritative sources

Find your disease.
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.

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

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

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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 1,301-1,320 of 10,888 diseases

atrial fibrillation, familial, 2

MONDO:0012167

Atrial fibrillation, familial, 2 is a form of an inherited cardiac rhythm disorder that primarily affects the electrical activity of the heart. Althou...

atrial fibrillation, familial, 3

MONDO:0011857

Atrial fibrillation, familial, 3 is an inherited cardiac condition characterized by abnormal electrical activity in the atria, leading to an irregular...

atrial fibrillation, familial, 4

MONDO:0012677

Atrial fibrillation, familial, 4 is an inherited cardiac rhythm disorder that primarily affects the electrical system of the heart, leading to irregul...

atrial fibrillation, familial, 5

MONDO:0012678

Atrial fibrillation, familial, 5 is a form of cardiac arrhythmia that runs in families and is characterized by an irregular heartbeat. It is inherited...

atrial fibrillation, familial, 6

MONDO:0012816

Atrial fibrillation, familial, 6 is an inherited cardiac condition primarily characterized by episodes of an irregular heartbeat. It is caused by muta...

atrial fibrillation, familial, 7

MONDO:0012828

Familial atrial fibrillation, familial, 7 is an inherited heart rhythm condition primarily affecting the electrical conduction system of the heart. It...

atrial fibrillation, familial, 8

MONDO:0013100

Atrial fibrillation, familial, 8 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

atrial fibrillation, familial, 9

MONDO:0013513

Atrial fibrillation, familial, 9 is an inherited heart rhythm disorder marked by episodes of irregular heartbeat. It is caused by mutations in the KCN...

atrial septal aneurysm

MONDO:0020438

Atrial septal aneurysm is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

atrial septal defect 1

MONDO:0007172

Atrial septal defect 1 is a type of congenital heart defect that involves an abnormal opening in the wall (septum) separating the two upper chambers o...

atrial septal defect 2

MONDO:0011938

Atrial septal defect 2 is a congenital heart condition characterized by an abnormal opening in the wall separating the heart’s two upper chambers. It...

atrial septal defect 3

MONDO:0013567

Atrial septal defect 3 is a congenital heart condition characterized by an abnormal opening in the wall that separates the heart’s two upper chambers....

atrial septal defect 4

MONDO:0012654

Atrial septal defect 4 is a congenital heart defect caused by mutations in the TBX20 gene that affects the wall separating the heart's upper chambers....

atrial septal defect 5

MONDO:0013011

Atrial septal defect 5 is a congenital cardiac condition characterized by an opening in the wall (septum) that separates the two atria of the heart. T...

atrial septal defect 6

MONDO:0013123

Atrial septal defect 6 is a congenital cardiac condition in which an opening in the atrial septum is present due to a mutation in the TLL1 gene. This...

atrial septal defect 7

MONDO:0007173

Atrial septal defect 7 is an extremely rare congenital heart condition that primarily affects the cardiovascular and respiratory systems. It is charac...

atrial septal defect 8

MONDO:0013750

Atrial septal defect 8 is a congenital heart condition characterized by an opening in the atrial septum resulting from a mutation in the CITED2 gene....

atrial septal defect 9

MONDO:0013770

Atrial septal defect 9 is a congenital heart defect that affects the structure of the atrial septum, the wall that separates the heart’s upper chamber...

atrial septal defect, coronary sinus type

MONDO:0020435

Atrial septal defect, coronary sinus type, is a specific form of atrial septal defect characterized by an abnormal opening between the heart's atria,...

atrial septal defect, ostium primum type

MONDO:0020437

Atrial septal defect, ostium primum type is a congenital heart defect characterized by an abnormal opening between the left and right atria resulting...

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