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Showing 5,061-5,080 of 15,964 diseases
MONDO:0003993
childhood vagina botryoid rhabdomyosarcoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is li...
MONDO:0035647
Childhood-onset Steinert myotonic dystrophy is an extremely rare condition. Because few cases have been documented, detailed clinical information is l...
MONDO:0018206
childhood-onset autosomal recessive myopathy with external ophthalmoplegia is an extremely rare condition. Because few cases have been documented, det...
MONDO:0044332
childhood-onset benign chorea with striatal involvement is an extremely rare condition. Because few cases have been documented, detailed clinical info...
MONDO:0020072
Childhood-onset epilepsy syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0800500
childhood-onset epilepsy syndrome with developmental and/or epileptic encephalopathy is an extremely rare condition. Because few cases have been docum...
MONDO:0800498
Childhood-onset genetic generalized epilepsy syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical inform...
MONDO:0800499
childhood-onset idiopathic generalized epilepsy syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical inf...
MONDO:0044701
Childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder is a severe neurodevelopmental condition that primarily...
MONDO:0015738
Childhood-onset nemaline myopathy is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0018759
childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome is an extremely rare condition. Because few cases have been do...
MONDO:0957430
Childhood-onset schizophrenia is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0800502
Childhood-onset self-limited focal epilepsy syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical informa...
MONDO:0012155
Choanal atresia (CA) is a congenital condition characterized by the obstruction of one or both choanal apertures, leading to varying degrees of respir...
MONDO:0015313
Choanal atresia, bilateral is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0015312
Choanal atresia, unilateral is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0035651
Choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome is a very rare multisystem condition that primarily affects structures o...
MONDO:0012064
Choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome, also called Burn-McKeown syndrome, is an extremely rare inherited cond...
MONDO:0019087
Cholangiocarcinoma is a type of carcinoma that arises from the bile ducts, affecting either the intrahepatic region or the area near the junction of t...
MONDO:0014281
Cholangiocarcinoma, susceptibility to is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited...