ataxia with neurogenic weakness and retinitis pigmentosa
ataxia with neurogenic weakness and retinitis pigmentosa
an ataxic syndrome associated with mutation in the mitochondrial gene coding for adenosine triphosphatase.
Medical browser
?
- ▲
- atactic agraphia
- atactiform
- atactilia
- Atalaya hemiglauca
- ataque de nervios
- ataractic
- ataralgesia
- Atarax
- ataraxia
- ataraxic
- atavism
- atavistic
- atavistic epiphysis
- atavistic foot
- atavistic regression
- ataxaphasia
- ataxia
- ataxia neuropathy spectrum
- ataxia of Charlevoix-Saguenay
- ataxia of early onset with retained reflexes
- ataxia paramyotonia
- ataxia telangiectasia
- ataxia telangiectasialike disorder
- ataxia with infantile onset olivopontocerebellar atrophy
- ataxia with isolated vitamin E deficiency
- ataxia with neurogenic weakness and retinitis pigmentosa
- ataxia with oculomotor apraxia type 1
- ataxia with oculomotor apraxia type 2
- ataxia with oculomotor apraxia, I & II
- ataxia, autosomal recessive, with deafness and optic atrophy
- ataxiadynamia
- ataxiagram
- ataxiagraph
- ataxia-hypogonadism
- ataxiameter
- ataxiamnesia
- ataxiaphasia
- ataxia-telangiectasia
- ataxia-telangiectasia syndrome
- ataxic
- ataxic aphasia
- ataxic breathing
- ataxic dysarthria
- ataxic gait
- ataxic paramyotonia
- ataxic paraplegia
- ataxic speech
- ataxin
- ataxiophemia
- ataxiophobia
- ataxophobia
- ▼
Full browser
?
- ▲
- ataxia
- ataxia
- ataxia
- ataxia
- ataxia 1, early onset with hypoalbuminaemia
- ataxia 1, early onset with hypoalbuminaemia
- ataxia cordis
- ataxia cordis
- ataxia cordis
- ataxia cordis
- ataxia neuropathy spectrum
- ataxia ocular apraxia-1
- ataxia of Charlevoix-Saguenay
- ataxia of early onset with retained reflexes
- ataxia paramyotonia
- ataxia telangiectasia
- ataxia telangiectasia
- Ataxia telangiectasia and Rad3 related
- Ataxia telangiectasia and Rad3 related
- Ataxia Telangiectasia and Rad3-related
- Ataxia telangiectasia and Rad3-related protein
- Ataxia telangiectasia and Rad3-related protein
- Ataxia Telangiectasia Children's Project
- Ataxia telangiectasia mutated
- Ataxia telangiectasia mutated
- ataxia telangiectasia syndrome
- ataxia telangiectasialike disorder
- ataxia with infantile onset olivopontocerebellar atrophy
- ataxia with isolated vitamin E deficiency
- ataxia with myoclonus
- ataxia with neurogenic weakness and retinitis pigmentosa
- ataxia with oculomotor apraxia type 1
- ataxia with oculomotor apraxia type 2
- ataxia with oculomotor apraxia, I & II
- Ataxia with Vitamin E Deficiency
- ataxia, autosomal recessive, with deafness and optic atrophy
- Ataxia, Friedreich-like, with selective vitamin E deciency
- ataxia, recessive, of Beauce
- Ataxia-Deafness-Retardation Syndrome
- ataxia-hypogonadism
- Ataxia-Microcephaly-Cataract syndrome
- Ataxia-Oculomotor Apraxia Syndrome
- Ataxia-telangiectasia
- Ataxia-telangiectasia
- Ataxia-telangiectasia
- Ataxia-telangiectasia
- ataxia-telangiectasia syndrome
- ataxia-telangiectasia variant
- Ataxia-Telangiectasia-Like Disorder
- ataxiadynamia
- ataxiagram
- ataxiagraph
- ataxiameter
- ataxiamnesia
- ataxiaphasia
- ataxic
- ataxic
- ataxic
- ataxic abasia
- ataxic abasia
- ataxic aphasia
- ▼