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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 4,261-4,280 of 10,888 diseases
MONDO:0022894
Craniosynostosis autosomal dominant is a condition affecting the skull in which the sutures fuse prematurely, potentially altering the shape of the he...
MONDO:0015468
Craniosynostosis-cataract syndrome is a condition that primarily affects the development of the skull and eyes. Although detailed descriptions are not...
MONDO:0022895
craniosynostosis cleft lip palate arthrogryposis is a rare disease. Detailed information about this condition is currently limited in medical literatu...
MONDO:0022896
Craniosynostosis contractures cleft is a condition that appears to involve abnormal skull development, joint contractures, and orofacial clefting. Alt...
MONDO:0007401
Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome is a complex malformation disorder that affects the skull and brain structures. It i...
MONDO:0022897
Craniosynostosis exostoses nevus epibulbar dermoid is a condition that appears to affect the development of the cranial bones and the ocular surface....
MONDO:0957473
Craniosynostosis-facial dysmorphism-chiari-1 malformation-developmental and language delay syndrome is a complex condition that affects the cranial st...
MONDO:0009038
Craniosynostosis-fibular aplasia syndrome is an extremely rare condition characterized by premature fusion of the cranial sutures along with the conge...
MONDO:0022890
Craniosynostosis Fontaine type is a condition that affects the normal development of the skull, often leading to an abnormal head shape due to the pre...
MONDO:0016291
Craniosynostosis, Herrmann-Opitz type is a rare bone development disorder that primarily affects the skull, facial structures, and limb formation. It...
MONDO:0015751
Craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome is a very rare condition that affects the development...
MONDO:0022898
Craniosynostosis intellectual disability heart defects is a condition that primarily affects the structure of the skull, cognitive development, and he...
MONDO:0012035
Craniosynostosis-intracranial calcifications syndrome, also known as Longman-Tolmie syndrome and craniosynostosis, calcification of basal ganglia, and...
MONDO:0022891
Craniosynostosis Maroteaux Fonfria type is a condition characterized by the premature fusion of one or more cranial sutures, which can affect the shap...
MONDO:0015467
Craniosynostosis, Philadelphia type is a syndromic form of craniosynostosis that primarily affects the skull and the hands and feet. It is characteriz...
MONDO:0011679
Craniosynostosis syndrome, autosomal recessive is a condition characterized by the premature fusion of skull bones, which can alter head shape and pot...
MONDO:0011347
Craniosynostosis with ectopia lentis is a condition that appears to involve abnormal skull development along with displacement of the eye lens. Althou...
MONDO:0012006
Craniosynostosis with ocular abnormalities and hallucal defects is a condition characterized by premature fusion of the skull bones accompanied by eye...
MONDO:0009042
Craniotelencephalic dysplasia is an extremely rare developmental disorder that affects the structure of the skull and brain. It is characterized by pr...
MONDO:0859226
Craniotubular dysplasia, Ikegawa type is a skeletal condition that primarily affects bone development and craniofacial structure. It is caused by chan...
Built from MONDO, HPO, ClinicalTrials.gov, FDA, Orphanet, and 7 more public sources. Updated daily.