Explore 10,888+ rare diseases with trusted, clear information
Medical professionals review and validate information.
Expert Stewards stand behind their work.
Patients and families contribute real-world insights.
Showing 4,801-4,820 of 15,964 diseases
MONDO:0011928
Caudal duplication (CD) is a rare developmental anomaly characterized by the duplication of structures derived from the embryonic cloaca and notochord...
MONDO:0017607
Caudal regression sequence is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0018639
Caudal regression-sirenomelia spectrum is an extremely rare condition. Because few cases have been documented, detailed clinical information is limite...
MONDO:0016146
Caveolinopathy is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0003155
Cavernous hemangioma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0003644
Cavernous hemangioma of colon is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0003645
Cavernous hemangioma of face is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0001975
Cavernous hemangioma of orbit is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0021281
Cavernous hemangioma of retina is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0002996
Cavernous sinus meningioma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0015623
Cavitary myiasis is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0002034
Cecum lymphoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited. It is classified as a...
MONDO:0006126
Cecum neuroendocrine tumor G1 is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0009187
Celiac disease-epilepsy-cerebral calcification syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical info...
MONDO:0017388
Celiac trunk compression syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0004454
Cellular congenital mesoblastic nephroma is an extremely rare condition characterized by increased cellularity, sheet-like proliferation of fibroblast...
MONDO:0003470
Cellular ependymoma is a variant of ependymoma characterized by a conspicuous increase in cellularity without a significant rise in mitotic activity....
MONDO:0800121
Cellular interstitial pneumonitis is an interstitial lung disease that manifests in infancy, with affected infants typically exhibiting breathing diff...
MONDO:0003305
Cellular neurofibroma is a type of neurofibroma characterized by areas with increased cellularity, representing a benign tumor that originates from ne...
MONDO:0004463
Cellular phase chronic idiopathic myelofibrosis is characterized by bone marrow hypercellularity and the presence of atypical megakaryocytes, without...