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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 9,441-9,460 of 10,888 diseases
MONDO:0014164
Meckel syndrome, type 11 is a rare genetic disorder caused by a mutation in the TMEM231 gene. This condition is one type within a group of disorders k...
MONDO:0011296
Meckel syndrome, type 2 is a rare condition caused by a mutation in the TMEM216 gene. It is one of the types of Meckel syndrome and is sometimes refer...
MONDO:0011821
Meckel syndrome, type 3 is a rare genetic disorder caused by a mutation in the TMEM67 gene. This condition is one type of Meckel syndrome, and its nam...
MONDO:0012626
Meckel syndrome, type 4 is a form of Meckel syndrome that is caused by a mutation in the CEP290 gene. This condition is defined by its genetic basis,...
MONDO:0012695
Meckel syndrome, type 5 is a rare genetic condition that is part of the group of disorders known as Meckel syndrome. This condition is defined by a mu...
MONDO:0012848
Meckel syndrome, type 6 is a rare inherited condition that is caused by a mutation in the CC2D2A gene. This condition is part of the group of disorder...
MONDO:0013482
Meckel syndrome, type 8 is a rare genetic condition that is caused by a mutation in the TCTN2 gene. This condition is part of the group of disorders k...
MONDO:0013630
Meckel syndrome, type 9 is a rare form of Meckel syndrome. This condition occurs when there is a mutation in the B9D1 gene. Meckel syndrome is a group...
MONDO:0006851
Meconium aspiration syndrome is a serious respiratory condition that occurs when a newborn inhales a mixture of meconium and amniotic fluid during or...
MONDO:0100000
MED12-related intellectual disability syndrome is an X-linked condition that causes intellectual disability and various other physical features. It is...
MONDO:0018929
Medial condensing osteitis of the clavicle is a condition characterized by abnormal changes in the medial portion of the clavicle, often involving inc...
MONDO:0016062
MONDO:0015413
MONDO:0003598
Median nerve neuropathy is a condition that affects the median nerve as it travels from the brachial plexus to the hand. It is characterized by weakne...
MONDO:0007904
MONDO:0003808
Mediastinal extraskeletal osteosarcoma is a cancer originating in the soft tissues of the mediastinum, the central area of the chest. As an osteosarco...
MONDO:0021067
Mediastinal germ cell tumor is a type of tumor that arises in the mediastinum, the central part of the chest. It encompasses a range of tumors includi...
MONDO:0003255
Mediastinal granular cell myoblastoma is an exceptionally rare and generally benign tumor that arises in the posterior mediastinum. The condition is c...
MONDO:0004020
Mediastinal gray zone lymphoma is a type of lymphoma located in the central chest area, known as the mediastinum. It is characterized by a blend of fe...
MONDO:0006298
Mediastinal malignant germ cell tumor is an extragonadal cancer arising in the mediastinum, a central compartment of the chest. It represents a hetero...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.