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Showing 6,921-6,940 of 10,888 diseases

early T cell progenitor acute lymphoblastic leukemia

MONDO:0100291

Rare

early congenital syphilis

MONDO:0000333

Rare

early invasive cervical adenocarcinoma

MONDO:0004530

Rare

1 Trials

early yaws

MONDO:0001067

Rare

Early yaws is an infection that progresses through primary and secondary stages, beginning with an initial lesion at the site of inoculation followed...

early-childhood-onset neurodegeneration with retinitis pigmentosa, sensorineural hearing loss, and demyelinating peripheral neuropathy

MONDO:0700288

Rare

1 Trials

KLC4

early-infantile DEE

MONDO:0800491

Rare

37 Trials

Early-infantile DEE is a neonatal/infantile epilepsy syndrome characterized by frequent drug-resistant seizures that begin at or before 3 months of ag...

SLC25A22SLC1A2SIK1

early-onset Lafora body disease

MONDO:0014717

Rare

Early-onset Lafora body disease is an extremely rare inherited neurological condition characterized by progressive myoclonus epilepsy and the formatio...

PRDM8

early-onset Parkinson disease 20

MONDO:0014233

Rare

SYNJ1

early-onset anterior polar cataract

MONDO:0020373

Rare

early-onset autoimmune disorder due to DOCK11 partial deficiency

MONDO:0958137

Rare

early-onset autoimmunity-autoinflammation-immunodeficiency syndrome

MONDO:0850068

Rare

early-onset autosomal dominant Alzheimer disease

MONDO:0015140

Rare

7 Trials

Early-onset autosomal dominant Alzheimer disease is a progressive form of dementia that primarily affects cognitive functions, such as memory and reas...

PSEN1APPPSEN2

early-onset calcifying leukoencephalopathy-skeletal dysplasia

MONDO:0034143

Rare

early-onset cerebellar ataxia with retained tendon reflexes

MONDO:0008938

Rare

1 Trials

early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation

MONDO:0017325

Rare

GRIN2A

early-onset familial hypoaldosteronism

MONDO:0035320

Rare

early-onset generalized dystonia

MONDO:0100016

Rare

Early-onset generalized dystonia is a neurological movement disorder that typically presents in childhood and is characterized by widespread involunta...

TOR1A

early-onset generalized limb-onset dystonia

MONDO:0007492

Rare

Early-onset generalized limb-onset dystonia is a rare movement disorder characterized by involuntary, sustained muscle contractions that lead to abnor...

TOR1A

early-onset immune dysregulation due to DOCK11 complete deficiency

MONDO:0958138

Rare

early-onset lamellar cataract

MONDO:0018611

Rare

Page 347 of 545

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