| Diseases |
Alias |
|
| Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes |
|
Melas Syndrome
|
MELAS
|
|
Mitochondrial Encephalomyopathy Lactic Acidosis And Stroke-Like Episodes
|
Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode
|
|
Mitochondrial Encephalomyopathy, Lactic Acidosis, And Stroke-Like Episodes
|
Myopathy, Mitochondrial-Encephalopathy-Lactic Acidosis-Stroke
|
|
Mitochondrial Encephalomyopathy, Lactic Acidosis And Stroke-Like Episodes
|
Mitochondrial Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes
|
|
Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis And Stroke-Like Episodes
|
Mitochondrial Encephalomyopathy With Lactic Acidosis And Stroke-Like Episodes Syndrome
|
|
Myopathy, Mitochondrial, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes
|
|
|
| Leber Hereditary Optic Neuropathy, Modifier Of |
|
Leber Optic Atrophy
|
Leber Hereditary Optic Neuropathy
|
|
LHON
|
Leber'S Hereditary Optic Neuropathy
|
|
Leber Optic Atrophy, Susceptibility To
|
Leber'S Optic Atrophy
|
|
LOAM
|
Loas
|
|
Leber'S Disease
|
Leber'S Optic Neuropathy
|
|
Optic Atrophy, Hereditary, Leber
|
Lhon, Modifier Of
|
|
Optic Atrophy, Leber Type
|
Hereditary Optic Neuroretinopathy
|
|
Leber Hereditary Optic Atrophy
|
Loa
|
|
Optic Atrophy Leber Type
|
Leber Hereditary Optic Neuropathy, Modifier
|
|
Leber Hereditary Optic Neuropathy Susceptibility
|
Modifier Of Leber Hereditary Optic Neuropathy
|
|
Lebers Hereditary Optic Neuropathy
|
Leber Congenital Amaurosis
|
|
|
| Leigh Syndrome |
|
Leigh Disease
|
Infantile Subacute Necrotizing Encephalopathy
|
|
Leigh Syndrome Due To Mitochondrial Complex Iv Deficiency
|
LS
|
|
Sne
|
Leigh'S Disease
|
|
Leigh Syndrome Due To Mitochondrial Complex I Deficiency
|
Necrotizing Encephalopathy, Infantile Subacute, Of Leigh
|
|
Subacute Necrotizing Encephalomyelopathy
|
Necrotizing Encephalopathy Infantile Subacute Of Leigh
|
|
Leigh Syndrome Due To Mitochondrial Complex Iii Deficiency
|
Infantile Necrotizing Encephalomyelopathy
|
|
Juvenile Subacute Necrotizing Encephalomyelopathy
|
Leigh'S Necrotizing Encephalopathy
|
|
Subacute Necrotizing Encephalopathy
|
Juvenile Subacute Necrotizing Encephalopathy
|
|
Leigh Syndrome Due To Mitochondrial Complex Ii Deficiency
|
Leigh Syndrome Due To Mitochondrial Complex V Deficiency
|
|
Encephalopathy, Subacute Necrotizing, Infantile
|
Encephalopathy, Subacute Necrotizing, Juvenile
|
|
Maternally Inherited Leigh Syndrome
|
Subacute Necrotising Encephalomyelopathy
|
|
Subacute Necrotising Encephalopathy
|
|
|
| Myoclonic Epilepsy Associated With Ragged-Red Fibers |
|
Merrf Syndrome
|
MERRF
|
|
Fukuhara Syndrome
|
Myoclonic Epilepsy Associated With Ragged Red Fibers
|
|
Myoencephalopathy Ragged-Red Fiber Disease
|
Myoclonic Epilepsy - Ragged Red Fibers
|
|
Myoclonus Epilepsy And Ragged Red Fibers
|
Myoclonus With Epilepsy And With Ragged Red Fibers
|
|
Myoclonic Epilepsy With Ragged Red Fibers
|
Myoclonic Epilepsy With Ragged-Red Fibers
|
|
Fukuhara Disease
|
Myoclonus Epilepsy Associated With Ragged-Red Fibres
|
|
Myoclonus With Epilepsy With Ragged Red Fibers
|
|
|
| Mitochondrial Disease |
|
Mitochondrial Diseases
|
Mitochondrial Disorder
|
|
|
| Mitochondrial Myopathy, Infantile, Transient |
|
Mitochondrial Myopathy With Reversible Cytochrome C Oxidase Deficiency
|
MMIT
|
|
Mitochondrial Myopathy, Infantile, Transient, Due To Respiratory Chain Deficiency
|
Cox Deficiency Myopathy, Infantile, Transient
|
|
Respiratory Chain Deficiency, Infantile, Transient
|
Benign Cox Deficiency
|
|
Infantile Reversible Cytochrome C Oxidase Deficiency Myopathy
|
Mitochondrial Myopathy With Reversible Cox Deficiency
|
|
Mitochondrial Myopathy With Reversible Complex Iv Deficiency
|
Reversible Infantile Cytochrome C Oxidase Deficiency
|
|
Reversible Infantile Respiratory Chain Deficiency
|
|
|
| Mitochondrial Dna-Associated Leigh Syndrome |
|
Mils
|
Maternally Inherited Leigh Syndrome
|
|
Leigh Disease, Maternally Inherited
|
Subacute Necrotizing Encephalomyelopathy Maternally Inherited
|
|
Maternally-Inherited Leigh Disease
|
Maternally-Inherited Infantile Subacute Necrotizing Encephalopathy
|
|
Mtdna-Associated Leigh Syndrome
|
|
|
| Leber Plus Disease |
|
Leber Congenital Amaurosis
|
Lca
|
|
Leber'S Amaurosis
|
Leber'S Disease
|
|
Amaurosis Congenita Of Leber
|
Amaurosis Congenita Of Leber, Type 1
|
|
Lhon Plus Disease
|
Congenital Absence Of The Rods And Cones
|
|
Congenital Retinal Blindness
|
Crb
|
|
Congenital Amaurosis Of Retinal Origin
|
Leber'S Congenital Amaurosis
|
|
Leber Congenital Amaurosis 1
|
Leber'S Congenital Tapetoretinal Degeneration
|
|
Leber'S Congenital Tapetoretinal Dysplasia
|
Lca1
|
|
Leber Congenital Amaurosis Type 1
|
Retinal Blindness, Congenital
|
|
Amaurosis, Leber Congenital
|
Dysgenesis Neuroepithelialis Retinae
|
|
Hereditary Epithelial Dysplasia Of Retina
|
Hereditary Retinal Aplasia
|
|
Heredoretinopathia Congenitalis
|
Leber Abiotrophy
|
|
Leber Congenital Tapetoretinal Degeneration
|
Lebers Congenital Amaurosis
|
|
Optic Atrophy, Hereditary, Leber
|
|
|
| Hereditary Optic Neuropathy |
|
|
| Parkinson Disease 6, Autosomal Recessive Early-Onset |
|
Autosomal Recessive Early-Onset Parkinson Disease 6
|
Parkinson Disease 6
|
|
PARK6
|
Parkinson Disease 6, Early Onset
|
|
Parkinson'S Disease 6
|
Parkinson Disease 6, Early-Onset
|
|
Autosomal Recessive Early-Onset Parkinson'S Disease 6
|
Early-Onset Parkinson Disease 6
|
|
Autosomal Recessive Early-Onset Parkinson Disease Type 6
|
Parkinson Disease 6 Early-Onset
|
|
Parkinson Disease 6 Late-Onset Susceptibility To
|
Parkinson Disease Autosomal Recessive Early-Onset Digenic Pink1/Dj1
|
|
Parkinsonism Young Adult Onset
|
Parkinson Disease, Autosomal Recessive Early-Onset, Digenic, Pink1/Dj1
|
|
Parkinson Disease, Type 6, Autosomal Recessive, Early-Onset
|
|
|
| Mitochondrial Encephalomyopathy |
|
Mitochondrial Encephalomyopathies
|
Encephalomyopathy, Mitochondrial
|
|
|
| Kearns-Sayre Syndrome |
|
Ophthalmoplegia
|
Mitochondrial Cytopathy
|
|
KSS
|
Ophthalmoplegia, Pigmentary Degeneration Of Retina, And Cardiomyopathy
|
|
Oculocraniosomatic Syndrome
|
Chronic Progressive External Ophthalmoplegia With Myopathy
|
|
Cpeo With Myopathy
|
Total Ophthalmoplegia
|
|
Ophthalmoplegia-Plus Syndrome
|
Ophthalmoplegia, Progressive External, With Ragged-Red Fibers
|
|
Cpeo With Ragged-Red Fibers
|
Oculomotor Paralysis
|
|
Renal Tubulopathy, Diabetes Mellitus, And Cerebellar Ataxia Due To Duplication O
|
Renal Tubulopathy, Diabetes Mellitus, And Cerebellar Ataxia Due To Duplication Of Mitochondrial Dna
|
|
Proximal Tubulopathy, Diabetes Mellitus And Cerebellar Ataxia
|
Cpeo With Ragged Red Fibers
|
|
Ophthalmoplegia Plus Syndrome
|
Ophthalmoplegia, Progressive External, With Ragged Red Fibers
|
|
Kearns-Sayre Mitochondrial Cytopathy
|
Mitochondrial Myopathies
|
|
|
| Progressive Myoclonus Epilepsy 9 |
|
Emp9
|
Pme Type 9
|
|
Progressive Myoclonic Epilepsy Due To Lmnb2 Deficiency
|
Progressive Myoclonus Epilepsy Type 9
|
|
|
| Neuropathy |
|
Peripheral Neuropathy
|
Peripheral Neuropathies
|
|
|
| Progressive Myoclonus Epilepsy 8 |
|
Emp8
|
Pme Type 8
|
|
Progressive Myoclonic Epilepsy Due To Cers1 Deficiency
|
Progressive Myoclonus Epilepsy Type 8
|
|
|
| Lactic Acidosis |
|
Acidosis, Lactic
|
Acidosis Lactic
|
|
|
| Severe Congenital Neutropenia 1 |
|
|
| Early Myoclonic Encephalopathy |
|
Myoclonic Epilepsy
|
Myoclonic Seizure
|
|
Epilepsies, Myoclonic
|
Epileptic Seizures - Myoclonic
|
|
Epileptic Seizures, Myoclonic
|
Myoclonia Epileptica
|
|
Myoclonic Seizure Disorder
|
Early Myoclonic Encephalopathy With Suppression-Bursts
|
|
|
| Cortical Blindness |
|
|
| Bile Acid Synthesis Defect, Congenital, 1 |
|
CBAS1
|
Congenital Bile Acid Synthesis Defect 1
|
|
3-Beta-Hydroxy-Delta-5-C27-Steroid Oxidoreductase Deficiency
|
Congenital Bile Acid Synthesis Defect Type 1
|
|
Basd1
|
Congenital Bile Acid Synthesis Defect, Type 1
|
|
3-Alpha Beta-Hydroxy-Delta-5-C27-Steroid Oxidoreductase, Deficiency Of
|
3beta-Hsdh Deficiency
|
|
3beta-Hydroxy-Delta-5-C27-Steroid Dehydrogenase Deficiency
|
3beta-Hydroxy-Delta-5-C27-Steroid Oxidoreductase Deficiency
|
|
Neonatal Progressive Intrahepatic Cholestasis
|
Pfic4
|
|
Progressive Familial Intrahepatic Cholestasis Type 4
|
Bile Acid Synthesis Defect, Congenital, Type 1
|
|
Cholestasis, Progressive Familial Intrahepatic 4
|
|
|
| Diphyllobothriasis |
|
Diphyllobothrium Infection
|
Fish Tapeworm
|
|
Bothriocephalosis
|
Infection By Bothriocephalus
|
|
Fish Tapeworm Infection
|
Dibothriocephalus Anaemia
|
|
Dibothriocephaliasis
|
Broad Tapeworm Infection
|
|
Bothriocephaliasis
|
Dibothriocephalus
|
|
Intestinal Diphyllobothriasis
|
Diphyllobothrium Infestation
|
|
Dibothriocephalus Infestation
|
Bothriocephalus Infestation
|
|
Adult Diphyllobothrium Infection
|
Tapeworm Anaemia
|
|
Infection By Diphyllobothrium Larvae
|
|
|
| Wolff-Parkinson-White Syndrome |
|
Wolff-Parkinson-White Pattern
|
Wpw Syndrome
|
|
Anomalous Atrioventricular Excitation
|
Anomalous A-V Excitation
|
|
Ventricular Pre-Excitation With Arrhythmia
|
WPWS
|
|
Ventricular Familial Preexcitation Syndrome
|
Preexcitation Syndrome
|
|
Ventricular Preexcitation
|
Wpw - [Wolff-Parkinson- White] Syndrome
|
|
Pre-Excitation Syndrome
|
|
|
| Leber Optic Atrophy And Dystonia |
|
LDYT
|
Marsden Syndrome
|
|
Leber Hereditary Optic Neuropathy With Dystonia
|
Leber Hereditary Optic Neuropathy And Dystonia
|
|
Familial Dystonia With Visual Failure And Striatal Lucencies
|
Dystonia, Familial, With Visual Failure And Striatal Lucencies
|
|
Leber Optic Atrophy With Dystonia
|
Dystonia Familial, With Visual Failure And Striatal Lucencies
|
|
Lhon And Dystonia
|
Leber'S Hereditary Optic Neuropathy With Dystonia
|
|
|
| Urocanase Deficiency |
|
Encephalopathy Due To Urocanase Deficiency
|
Urocanate Hydratase Deficiency
|
|
Urocanic Aciduria
|
UROCD
|
|
High Urine Urocanic Acid Levels
|
|
|
| Parkinsonism |
|
Parkinsonism-Plus
|
Idiopathic Parkinsonism
|
|
Primary Parkinsonism
|
Paralysis Agitans Syndrome
|
|
Parkinsonian Syndrome
|
Trembling Paralysis
|
|
Paralysis Agitans
|
Shaking Palsy
|
|
Shaking Paralysis
|
|
|
| Sparganosis |
|
Infection By Sparganum
|
Larval Diphyllobothriasis
|
|
Spirometrosis
|
Infection By Spirometra Larvae
|
|
Larval Dibothriocephaliasis
|
Sparganosis - Larval Diphyllobothriasis
|
|
Spirometriosis
|
Larval Dibothriocephalus Infestation
|
|
Larval Diphyllobothrium Infestation
|
Larval Dibothriocephalus
|
|
Infection Due To Sparganum
|
Larval Fish Tapeworm Infection
|
|
Spirometra Larvae Infestation
|
Sparganum Infestation
|
|
Larval Bothriocephalus Infestation
|
|
|
| Cystic Echinococcosis |
|
Echinococcus Granulosus Infection
|
Echinococcus Granulosus Infection Of Lung
|
|
Echinococcus Granulosus
|
Echinococcus Granulosus Infection Of Thyroid
|
|
Echinococcus Granulosus Infectious Disease
|
Echinococcus Granulosus Infectious Disease Of Liver
|
|
Echinococcus Granulosus Infectious Disease Of Thyroid
|
Liver Echinococcus Granulosus
|
|
Lung Echinococcus Granulosus
|
Thyroid Echinococcus Granulosus
|
|
Unilocular Echinococcosis
|
Unilocular Hydatid Disease
|
|
Hydatid Disease
|
Hydatidosis
|
|
Echinococcosis
|
|
|
| Coloboma, Ocular, With Or Without Hearing Impairment, Cleft Lip/Palate, And/Or Mental Retardation |
|
Uveal Coloboma-Cleft Lip And Palate-Intellectual Disability
|
COB1
|
|
Coloboma-Microphthalmos Syndrome
|
Coloboma-Microphthalmos Syndrome Associated With Sensorineural Hearing Loss, Hematuria, And Cleft Lip/Palate
|
|
Coloboma, Cleft Lip-Palate And Mental Retardation Syndrome
|
Ocular Coloboma With Or Without Hearing Impairment, Cleft Lip/Palate, And/Or Mental Retardation
|
|
Uveal Coloboma-Cleft Lip/Palate-Mental Retardation Syndrome
|
Uveal Coloboma-Cleft Lip/Palate-Intellectual Disability Syndrome
|
|
Coloboma, Ocular, With Or Without Hearing Impairment, Cleft Lip/Palate, And/Or Intellectual Disability
|
Coloboma, Ocular, With/Without Hearing Impairment, Cleft Lip/Palate, And/Or Mental Retardation
|
|
|
| Ancylostomiasis |
|
Ankylostomiasis
|
Hookworm Infection
|
|
Hookworm Infections
|
Ancylostomiasis Due To Ancylostoma Duodenale
|
|
Ancylostoma Duodenale Infection
|
|
|
| Cercarial Dermatitis |
|
Swimmer'S Itch
|
Cutaneous Schistosomiasis
|
|
Sea Bather'S Eruption
|
Clam-Digger'S Itch
|
|
Rice-Paddy Itch
|
Sea Bather'S Itch
|
|
Sawah Itch
|
Schistosomal Cercarial Dermatitis
|
|
|
| Dicrocoeliasis |
|
Disease Due To Dicrocoeliidae
|
Lancet Fluke Infection
|
|
Dicroceliosis
|
Lancet Fluke Disease
|
|
Lancet Fluke Infestation
|
|
|
| Taeniasis |
|
Beef Tapeworm Infection
|
Infection By Taeniarhynchus Saginatus
|
|
Taenia Saginata Infectious Disease
|
Taenia Saginata Infection
|
|
Pork Tapeworm Infection
|
Armed Tapeworm Infection
|
|
Infection By Taenia Solium
|
Intestinal Taenia Solium Infection
|
|
Pork Tapeworm
|
Taenia Solium Taeniasis
|
|
Adult Pork Tapeworm Infection
|
Adult Pork Tapeworm
|
|
Beef Tapeworm
|
Infection By Taenia Saginata
|
|
Unarmed Tapeworm Infection
|
Taenia Saginata Taeniasis
|
|
Infection Due To Adult Tapeworm Taenia Saginata
|
Mediocanellata Taenia Infection
|
|
Infestation By Taenia Saginata
|
Infestation By Taenia Mediocanellata
|
|
|
| Coenurosis |
|
|
| Myiasis |
|
Infestation By Fly Larvae
|
Infestation By Maggots
|
|
Maggot Infestation
|
Infestation By Larvae Of Flies
|
|
Infestation By Dermatobia
|
Infestation By Estrus Ovis
|
|
Infestation By Oestrus Ovis
|
Oestriasis
|
|
Oestrosis
|
|
|
| Mitochondrial Metabolism Disease |
|
Abnormality Of Mitochondrial Metabolism
|
Mitochondrial Diseases
|
|
|
| Cysticercosis |
|
Neurocysticercosis
|
Submacular Cysticercosis
|
|
Intestinal Taenia Solium Infection
|
Pork Tapeworm Infection
|
|
Tapeworm Infection: Intestinal Taenia Solum
|
Tapeworm Infection: Pork
|
|
Tenia Solium Infectious Disease
|
Taeniasis
|
|
Tenia Solium Infection
|
Cysticerciasis Infection Due To Larval Form Of Taenia Solium
|
|
|
| Renal Oncocytoma |
|
Oncocytoma, Renal
|
Oncocytoma Of Kidney
|
|
Renal Epithelial Oncocytic Tumor
|
Oncocytoma Kidney
|
|
Oncocytoma Renal
|
Kidney Oncocytoma
|
|
|
| Mitochondrial Myopathy |
|
Mitochondrial Myopathies
|
Mitochondrial Cytopathy
|
|
Myopathies In Mitochondrial Disorders
|
|
|
| Mitochondrial Dna Depletion Syndrome 4a |
|
Alpers Syndrome
|
Alpers-Huttenlocher Syndrome
|
|
Alpers Progressive Infantile Poliodystrophy
|
Alpers Diffuse Degeneration Of Cerebral Gray Matter With Hepatic Cirrhosis
|
|
Alpers Disease
|
Progressive Sclerosing Poliodystrophy
|
|
Pndc
|
Diffuse Cerebral Sclerosis Of Schilder
|
|
MTDPS4A
|
Neuronal Degeneration Of Childhood With Liver Disease, Progressive
|
|
Alper'S Syndrome
|
Alpers' Disease Or Gray-Matter Degeneration
|
|
Diffuse Cerebral Degeneration In Infancy
|
Infantile Poliodystrophy
|
|
Poliodystrophia Cerebri Progressiva
|
Progressive Cerebral Poliodystrophy
|
|
Alpers' Disease
|
Alpers Progressive Sclerosing Poliodystrophy
|
|
Progressive Neuronal Degeneration Of Childhood With Liver Disease
|
Ahs
|
|
Mitochondrial Dna Depletion Syndrome 4a Alpers Type
|
Neuronal Degeneration Of Childhood With Liver Disease Progressive
|
|
|
| Optic Nerve Disease |
|
Optic Neuropathy
|
Disorder Of The Second Nerve
|
|
Optic Nerve Disorder
|
Optic Nerve
|
|
Abnormality Of The Optic Nerve
|
Optic Nerve Disorders
|
|
Neuropathy, Optic
|
Disorder Of The Optic Nerve
|
|
|
| Cranial Nerve Disease |
|
Cranial Nerve Disorder
|
Disorder Of Cranial Nerve
|
|
Cranial Nerve Diseases
|
|
|
| Mitochondrial Dna Depletion Syndrome |
|
|
| Progressive Myoclonus Epilepsy |
|
Pme
|
Progressive Myoclonic Epilepsy
|
|
Myoclonic Epilepsies, Progressive
|
Unverricht-Lundborg Syndrome
|
|
|
| Parkinson Disease, Late-Onset |
|
Parkinson Disease
|
Parkinson'S Disease
|
|
PD
|
PARK
|
|
Parkinson Disease, Susceptibility To
|
Late Onset Parkinson'S Disease
|
|
Late Onset Parkinson Disease
|
Paralysis Agitans
|
|
Primary Parkinsonism
|
Idiopathic Parkinson Disease
|
|
Parkinson'S
|
Parkinson Disease, Late-Onset, Susceptibility To
|
|
Parkinson Disease, Age Of Onset, Modifier
|
Lewy Body Parkinson Disease
|
|
Idiopathic Parkinson'S Disease
|
Pd - [Parkinson Disease]
|
|
Parkinson Disease Nos
|
Parkinson, Nos
|
|
Primary Parkinson Disease
|
|
|
