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Showing 3,621-3,640 of 15,964 diseases
MONDO:0004280
Asymmetric motor neuropathy is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0000259
Asymptomatic dengue is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0975918
Asymptomatic hyperckemia-myalgia-rhabdomyolysis syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical inf...
MONDO:0000927
Asymptomatic neurosyphilis is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0008838
Ataxia – deafness – intellectual disability syndrome is an uncommon neurodevelopmental condition that affects the brain, inner ear, and coordination p...
MONDO:0014419
Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome, also called Poretti-Boltshauser syndrome, is a neuro-ophthalmological con...
MONDO:0014557
Ataxia - oculomotor apraxia type 4 is a very rare neurological condition characterized by difficulties with movement coordination and eye movement, an...
MONDO:0018266
Ataxia-telangiectasia variant is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0010781
Ataxia and polyneuropathy, adult-onset is an extremely rare condition. Because few cases have been documented, detailed clinical information is limite...
MONDO:0016798
Ataxia neuropathy spectrum is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0008840
Ataxia telangiectasia (AT) is a rare, multi-system neurological and immunologic condition that typically begins in early childhood. It is caused by ch...
MONDO:0007166
Ataxia with fasciculations is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.
MONDO:0014084
Ataxia with oculomotor apraxia type 3 is an inherited neurological condition that primarily affects coordination, eye movements, and motor control. It...
MONDO:0008842
Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia is a rare autosomal recessive cerebellar ataxia that primarily affects the coordinati...
MONDO:0008980
Ataxia-hypogonadism-choroidal dystrophy syndrome is a very rare neurodegenerative disorder that affects multiple systems, particularly the nervous, vi...
MONDO:0008038
Ataxia-pancytopenia syndrome is a very rare inherited disorder, seen in fewer than one in a million people, that affects both the brain and the bone m...
MONDO:0015248
Ataxia-photosensitivity-short stature syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical information i...
MONDO:0010095
Ataxia-tapetoretinal degeneration syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical information is li...
MONDO:0008841
Ataxia-telangiectasia with generalized skin pigmentation and early death is an extremely rare condition. Because few cases have been documented, detai...
MONDO:0011457
Ataxia-telangiectasia-like disorder is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.