Asphyxiating thoracic dystrophy 2, also known as ATD2 or IFT80 Jeune syndrome, is a form of skeletal dysplasia primarily affecting the development of...

Asphyxiating thoracic dystrophy 3 is a skeletal condition that affects the development of the chest and other structures, and is part of a group of di...

Asphyxiating thoracic dystrophy 4 is a skeletal and multisystem condition characterized by a narrow chest and shortened long bones, along with kidney...

Asphyxiating thoracic dystrophy 5 is an inherited skeletal dysplasia that affects multiple organ systems, including the respiratory, renal, ocular, an...

Astley-Kendall dysplasia is a lethal skeletal dysplasia that primarily affects bone and cartilage development, manifesting with markedly short limbs,...

Astrakhan spotted fever is an infectious disease reported in the Astrakhan region, Chad, and Kosovo. It is caused by infection with the bacterium rick...

Astroblastoma is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

astroblastoma, MN1-altered is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Astrocytoma, IDH-mutant, grade 2 is a tumor of the central nervous system characterized by the presence of well-differentiated fibrillary glial cells...

Astrocytoma, IDH-mutant, grade 3 is an aggressive brain tumor that arises from astrocytes and is characterized by increased cell division and anaplast...

Astrocytoma, IDH-mutant, grade 4 is a high-grade brain tumor that affects the central nervous system. It is characterized by pathological features suc...

Asymmetric motor neuropathy is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Asymptomatic dengue is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Asymptomatic hyperckemia-myalgia-rhabdomyolysis syndrome is an extremely rare condition. Because few cases have been documented, detailed clinical inf...

Asymptomatic neurosyphilis is an extremely rare condition. Because few cases have been documented, detailed clinical information is limited.

Ataxia and polyneuropathy, adult-onset is an extremely rare condition. Because few cases have been documented, detailed clinical information is limite...

Ataxia – deafness – intellectual disability syndrome is an uncommon neurodevelopmental condition that affects the brain, inner ear, and coordination p...

Ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia is a rare autosomal recessive cerebellar ataxia that primarily affects the coordinati...

Ataxia-hypogonadism-choroidal dystrophy syndrome is a very rare neurodegenerative disorder that affects multiple systems, particularly the nervous, vi...

Ataxia-intellectual disability-oculomotor apraxia-cerebellar cysts syndrome, also called Poretti-Boltshauser syndrome, is a neuro-ophthalmological con...