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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 9,381-9,400 of 10,888 diseases
MONDO:0017917
MONDO:0016366
Maternal phenylketonuria is a metabolic condition that occurs when a mother with high phenylalanine levels affects the development of her nonphenylket...
MONDO:0014013
Maternal riboflavin deficiency is a condition related to insufficient levels of the vitamin riboflavin in the mother's body, most likely due to dietar...
MONDO:0016651
Maternal uniparental disomy of chromosome 1 is a chromosomal anomaly in which both copies of chromosome 1 are inherited from the mother rather than on...
MONDO:0019994
MONDO:0019915
Maternal uniparental disomy of chromosome 14 is a chromosomal anomaly that results from both copies of chromosome 14 being inherited from the mother,...
MONDO:0019916
Maternal uniparental disomy of chromosome 16 is a condition in which both copies of chromosome 16 are inherited from the mother, leading to an imbalan...
MONDO:0019910
Maternal uniparental disomy of chromosome 2 is a genetic phenomenon in which both copies of chromosome 2 are inherited from the mother. In most cases,...
MONDO:0019917
Maternal uniparental disomy of chromosome 20 is a very rare chromosomal anomaly in which both copies of chromosome 20 are inherited from the mother, l...
MONDO:0019918
Maternal uniparental disomy of chromosome 21 is a rare chromosomal phenomenon in which both copies of chromosome 21 are inherited from the mother rath...
MONDO:0019919
Maternal uniparental disomy of chromosome 22 is a condition in which both copies of chromosome 22 are inherited from the mother, leading to an abnorma...
MONDO:0019911
Maternal uniparental disomy of chromosome 4 is a genetic event in which both copies of chromosome 4 are inherited from the mother. In itself, this unu...
MONDO:0019912
Maternal uniparental disomy of chromosome 6 is a genetic condition where both copies of chromosome 6 are inherited from the mother. This condition is...
MONDO:0019914
Maternal uniparental disomy of chromosome 9 is a chromosomal anomaly where both copies of chromosome 9 are inherited from the mother. In most instance...
MONDO:0016851
Maternal uniparental disomy of chromosome X is a genetic condition that results from inheriting both copies of the X chromosome exclusively from the m...
MONDO:0011010
Matthew-Wood syndrome is a rare condition that mainly affects the eyes and lungs. People with this condition may have very small eyes (severe micropht...
MONDO:0004467
Mature gastric teratoma is a benign tumor arising from the stomach, characterized by the presence of well-differentiated tissues derived from various...
MONDO:0003820
Mature ovarian teratoma is a benign ovarian tumor composed entirely of well-differentiated, adult-type tissues and is usually cystic in nature. It is...
MONDO:0004432
Mature pericardial teratoma is a benign tumor that arises from the pericardium, the sac-like structure surrounding the heart. This condition is genera...
MONDO:0000430
Mature T-cell and NK-cell non-Hodgkin lymphoma (NHL) encompasses a group of aggressive hematopoietic neoplasms, primarily affecting T-cells and natura...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.