| Diseases |
Alias |
|
| Mitochondrial Myopathy, Infantile, Transient |
-
Mitochondrial Myopathy With Reversible Cytochrome C Oxidase Deficiency
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MMIT
-
Mitochondrial Myopathy, Infantile, Transient, Due To Respiratory Chain Deficiency
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Cox Deficiency Myopathy, Infantile, Transient
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Respiratory Chain Deficiency, Infantile, Transient
-
Benign Cox Deficiency
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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
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Reversible Infantile Respiratory Chain Deficiency
|
|
| Diabetes And Deafness, Maternally Inherited |
-
MIDD
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Maternally Inherited Diabetes And Deafness
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Diabetes-Deafness Syndrome, Maternally Transmitted
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Ballinger-Wallace Syndrome
-
Diabetes Mellitus, Type Ii, With Deafness
-
Noninsulin-Dependent Diabetes Mellitus With Deafness
-
Niddm With Deafness
-
Diabetes-Deafness Syndrome Maternally Transmitted
-
Ballinger Wallace Syndrome
-
Diabetes Mellitus Type Ii With Deafness
-
Maternally Transmitted Diabetes-Deafness Syndrome
-
Mitochondrial Inherited Diabetes And Deafness
-
Maternally-Inherited Diabetes And Deafness
-
Maternally-Inherited Diabetes And Hearing Loss
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Mitochondrial Diabetes
|
|
| Mitochondrial Myopathy With Diabetes |
-
Mitochondrial Myopathy, Lipid Type
-
Myopathy And Diabetes Mellitus
-
Myopathy, Mitochondrial, With Diabetes Mellitus
|
|
| Gonadal Dysgenesis |
|
|
| Mitochondrial Myopathy |
|
|
| 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
|
|
| Mitochondrial Disease |
-
Mitochondrial Diseases
-
Mitochondrial Disorder
|
|
| Aceruloplasminemia |
-
Cerebellar Ataxia
-
Hypoceruloplasminemia
-
Hemosiderosis, Systemic, Due To Aceruloplasminemia
-
Familial Apoceruloplasmin Deficiency
-
Hereditary Ceruloplasmin Deficiency
-
Deficiency Of Ferroxidase
-
Hypoceruloplasminemia, Hereditary
-
Ceruloplasmin Deficiency
-
Systemic Hemosiderosis Due To Aceruloplasminemia
-
ACERULOP
|
|
| Dicrocoeliasis |
|
|
| Echinostomiasis |
|
|
| Fasciolopsiasis |
-
Infection By Fasciolopsis Buski
-
Infectious Disease By Fasciolopsis
-
Intestinal Distomatosis
-
Intestinal Distoma
-
Giant Intestinal Fluke Infection
-
Fasciolopsis Buski Infection
-
Infection By Fasciolopsis
-
Busk Fluke Infection
-
Intestinal Fluke Infestation
-
Infestation By Fasciolopsis
-
Intestinal Distomiasis
-
Intestinal Fluke Disease
-
Intestinal Fluke Infection
|
|
| Noonan Syndrome 1 |
-
Noonan Syndrome
-
NS1
-
Male Turner Syndrome
-
Female Pseudo-Turner Syndrome
-
Turner Phenotype With Normal Karyotype
-
Noonan Syndrome With Pigmented Villonodular Synovitis
-
Turner'S Phenotype, Karyotype Normal
-
Familial Turner Syndrome
-
Noonan'S Syndrome
-
Noonan-Ehmke Syndrome
-
Ns
-
Pseudo-Ullrich-Turner Syndrome
-
Turner Syndrome In Female With X Chromosome
-
Turner-Like Syndrome
-
Ullrich-Noonan Syndrome
-
Noonan-Like/Multiple Giant Cell Lesion Syndrome
-
Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions
-
Pterygium Colli Syndrome
-
Noonan Syndrome, Type 1
-
Turner Syndrome, Male
|
|
| 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
|
|
| Breast Cancer |
-
Breast Carcinoma
-
Male Breast Cancer
-
Breast Cancer, Familial
-
Malignant Neoplasm Of Breast
-
Breast Cancer, Susceptibility To
-
Breast Cancer, Early-Onset
-
Malignant Tumor Of Breast
-
Carcinoma Of Male Breast
-
Breast Cancer, Invasive Ductal
-
Breast Cancer, Protection Against
-
Breast Cancer, Somatic
-
Breast Cancer, Male
-
Breast Cancer, Lobular, Somatic
-
Breast Tumor
-
Mammary Cancer
-
Mammary Tumor
-
Malignant Neoplasm Of Male Breast
-
Mammary Carcinoma
-
Male Breast Carcinoma
-
Familial Cancer Of Breast
-
Invasive Ductal Breast Carcinoma
-
Breast Cancer Susceptibility
-
Breast Cancer, Male, Susceptibility To
-
Breast Cancer, Early-Onset, Susceptibility To
-
Malignant Tumor Of The Breast
-
Mammary Neoplasm
-
Primary Breast Cancer
-
Neoplasm Of Male Breast
-
Carcinoma Of Breast
-
Breast Cancer In Men
-
Familial Breast Cancer
-
Cancer Of Breast
-
BC
-
Breast Cancer Familial
-
Breast Cancer Familial Male
-
Breast Cancer, Familial Male
-
Breast Male Carcinoma
-
Breast Neoplasms
-
Breast Neoplasms, Male
-
Mammary Tumors
-
Mammary Carcinomas
-
Cancer, Breast
-
Cancer, Breast, Susceptibility
-
Invasive Breast Ductal Carcinoma
-
Breast Neoplasm
-
Susceptibility To Breast Cancer
-
Mammary Neoplasms
-
Animal Mammary Neoplasms
-
Primary Malignant Neoplasm Of Breast
-
Infiltrating Ductal Carcinoma Of Breast
-
Infiltrating Duct Carcinoma Of Unspecified Site
-
Infiltrating Ductular Carcinoma Of Unspecified Site
-
Invasive Breast Carcinoma Of No Special Type
-
Microinvasive Carcinoma Of Breast
-
Carcinoma With Apocrine Differentiation
|
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