Hereditary Sensory and Autonomic Neuropathies. Acroosteolysis, Giaccai Type . Acroosteolysis, Neurogenic . Congenital Insensitivity to Pain with Anhidrosis . Familial Dysautonomia, Type 2 . Familial Dysautonomia, Type II . Giaccai Type Acroosteolysis . HSAN (Hereditary Sensory Autonomic Neuropathy) . HSAN 1 . HSAN 4 . HSAN 5 . HSAN I . HSAN IV . HSAN V . HSAN2 . HSAN5 . HSANII . Hereditary Sensory And Autonomic Neuropathy IV . Hereditary Sensory Autonomic Neuropathy, Type 1 . Hereditary Sensory Autonomic Neuropathy, Type 2 . Hereditary Sensory Autonomic Neuropathy, Type 4 . Hereditary Sensory Autonomic Neuropathy, Type 5 . Hereditary Sensory Neuropathy Type 1 . Hereditary Sensory Neuropathy Type I . Hereditary Sensory Neuropathy Type Ia . Hereditary Sensory Radicular Neuropathy . Hereditary Sensory Radicular Neuropathy, Recessive Form . Hereditary Sensory and Autonomic Neuropathy 4 . Hereditary Sensory and Autonomic Neuropathy Type 1 . Hereditary Sensory and Autonomic Neuropathy Type 2 . Hereditary Sensory and Autonomic Neuropathy Type I . Hereditary Sensory and Autonomic Neuropathy Type II . Hereditary Sensory and Autonomic Neuropathy Type IV . Hereditary Sensory and Autonomic Neuropathy Type V . Hereditary Sensory and Autonomic Neuropathy, Type 4 . Hereditary Sensory and Autonomic Neuropathy, Type 5 . Insensitivity to Pain, Congenital, with Anhidrosis . Neurogenic Acroosteolysis . Neuropathy Hereditary Sensory Radicular, Autosomal Dominant . Neuropathy Hereditary Sensory and Autonomic Type 1 . Neuropathy, Congenital Sensory . Neuropathy, Congenital Sensory, with Anhidrosis . Neuropathy, Hereditary Sensory And Autonomic, Type I . Neuropathy, Hereditary Sensory And Autonomic, Type V . Neuropathy, Hereditary Sensory Radicular, Autosomal Dominant . Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive . Neuropathy, Hereditary Sensory, Type I . Neuropathy, Progressive Sensory, Of Children . Acroosteolyses, Neurogenic . Congenital Sensory Neuropathies . Congenital Sensory Neuropathy . HSANs (Hereditary Sensory Autonomic Neuropathy) . HSN Type IIs . Hereditary Sensory Neuropathies . Hereditary Sensory Neuropathy . Neurogenic Acroosteolyses . Neuropathies, Congenital Sensory . Neuropathies, Hereditary Sensory . Neuropathy, Hereditary Sensory . Sensory Neuropathies, Congenital . Sensory Neuropathies, Hereditary . Sensory Neuropathy, Congenital . Type I, HSAN . Type I, HSN . Type IV, HSAN . Neuropathies, Hereditary Sensory and Autonomic . HSAN 13449 . HSAN Type I . HSAN Type II . HSAN Type IV . HSAN Type V . HSN Type I . HSN Type II . Sensory and Autonomic Neuropathies, Hereditary . Sensory Neuropathy, Hereditary . Insensitivity to Pain with Anhidrosis, Congenital . Pain Insensitivity with Anhidrosis, Congenital . 1.00
Barth Syndrome. 3-Methylglutaconic Aciduria, Type II . 3-Methylglutaconicaciduria Type 2 . 3-Methylglutaconicaciduria Type II . Cardioskeletal Myopathy with Neutropenia and Abnormal Mitochondria . MGA Type 2 . MGA Type II . 3 Methylglutaconic Aciduria, Type II . 3 Methylglutaconicaciduria Type 2 . 3-Methylglutaconicaciduria Type 2s . 3-Methylglutaconicaciduria Type IIs . MGA Type 2s . MGA Type IIs . Syndrome, Barth . Type 2, 3-Methylglutaconicaciduria . Type 2, MGA . Type 2s, MGA . Type II, MGA . Type IIs, MGA . MGA type II . 3-methylglutaconicaciduria type 2 . 3-methylglutaconicaciduria type II . 0.58
Hyperlipoproteinemia Type II. Apolipoprotein B-100, Familial Defective . Apolipoprotein B-100, Familial Ligand-Defective . Familial Combined Hyperlipoproteinemia . Hyper-Low Density Lipoproteinemia . Hyper-Low-Density-Lipoproteinemia . Hyper-beta-Lipoproteinemia . Hypercholesterolemia, Autosomal Dominant . Hypercholesterolemia, Autosomal Dominant, Type B . Hypercholesterolemic Xanthomatosis, Familial . Hyperlipoproteinemia Type 2 . Hyperlipoproteinemia Type IIa . Hyperlipoproteinemia Type IIb . Hyperlipoproteinemia, Type II . Hyperlipoproteinemia, Type IIa . LDL Receptor Disorder . Apolipoprotein B 100, Familial Defective . Apolipoprotein B 100, Familial Ligand Defective . Autosomal Dominant Hypercholesterolemia . Autosomal Dominant Hypercholesterolemias . Combined Hyperlipoproteinemia, Familial . Combined Hyperlipoproteinemias, Familial . Density Lipoproteinemia, Hyper-Low . Density Lipoproteinemias, Hyper-Low . Disorder, LDL Receptor . Disorders, LDL Receptor . Dominant Hypercholesterolemia, Autosomal . Dominant Hypercholesterolemias, Autosomal . Essential Hypercholesterolemia . Essential Hypercholesterolemias . Familial Combined Hyperlipoproteinemias . Familial Hypercholesterolemia . Familial Hypercholesterolemias . Familial Hypercholesterolemic Xanthomatoses . Familial Hypercholesterolemic Xanthomatosis . Hyper Low Density Lipoproteinemia . Hyper beta Lipoproteinemia . Hyper-Low Density Lipoproteinemias . Hyper-Low-Density-Lipoproteinemias . Hyper-beta-Lipoproteinemias . Hyperbetalipoproteinemias . Hypercholesterolemias, Autosomal Dominant . Hypercholesterolemias, Essential . Hypercholesterolemias, Familial . Hypercholesterolemic Xanthomatoses, Familial . Hyperlipoproteinemia Type 2s . Hyperlipoproteinemia Type IIas . Hyperlipoproteinemia Type IIbs . Hyperlipoproteinemia Type IIs . Hyperlipoproteinemia, Familial Combined . Hyperlipoproteinemias, Familial Combined . Hyperlipoproteinemias, Type II . Hyperlipoproteinemias, Type IIa . LDL Receptor Disorders . Lipoproteinemia, Hyper-Low Density . Lipoproteinemias, Hyper-Low Density . Receptor Disorder, LDL . Receptor Disorders, LDL . Type 2, Hyperlipoproteinemia . Type II Hyperlipoproteinemia . Type II Hyperlipoproteinemias . Type IIa Hyperlipoproteinemia . Type IIa Hyperlipoproteinemias . Xanthomatoses, Familial Hypercholesterolemic . Xanthomatosis, Familial Hypercholesterolemic . Hypercholesterolemia, Familial . Hyperbetalipoproteinemia . Hypercholesterolemia, Essential . 0.54
Glycogen Storage Disease Type II. Acid Alpha-Glucosidase Deficiency . Acid Maltase Deficiency . Adult Glycogen Storage Disease Type II . Alpha-1,4-Glucosidase Deficiency . Deficiency Disease, Acid Maltase . Deficiency Disease, Lysosomal alpha-1,4-Glucosidase . Deficiency of Alpha-Glucosidase . GAA Deficiency . GSD II . GSD2 13663 . Glycogen Storage Disease II . Glycogen Storage Disease Type 2 . Glycogen Storage Disease Type II, Adult . Glycogen Storage Disease Type II, Infantile . Glycogen Storage Disease Type II, Juvenile . Glycogenosis Type II . Infantile Glycogen Storage Disease Type II . Juvenile Glycogen Storage Disease Type II . Pompe's Disease . Acid Alpha Glucosidase Deficiency . Acid Alpha-Glucosidase Deficiencies . Acid Maltase Deficiencies . Alpha 1,4 Glucosidase Deficiency . Alpha-1,4-Glucosidase Deficiencies . Alpha-Glucosidase Deficiencies . Alpha-Glucosidase Deficiencies, Acid . Alpha-Glucosidase Deficiency . Alpha-Glucosidase Deficiency, Acid . Deficiencies, Acid Alpha-Glucosidase . Deficiencies, Acid Maltase . Deficiencies, Alpha-1,4-Glucosidase . Deficiencies, GAA . Deficiency of Alpha Glucosidase . Deficiency, Acid Alpha-Glucosidase . Deficiency, Acid Maltase . Deficiency, Alpha-1,4-Glucosidase . Deficiency, GAA . Disease, Pompe . Disease, Pompe's . GAA Deficiencies . GSD2s . Generalized Glycogenoses . Glycogenoses, Generalized . Glycogenosis, Generalized . Lysosomal alpha 1,4 Glucosidase Deficiency Disease . Maltase Deficiencies, Acid . Pompes Disease . Type II, Glycogenosis . Type IIs, Glycogenosis . Generalized Glycogenosis . Glycogenosis 2 . Pompe Disease . Acid Maltase Deficiency Disease . Lysosomal alpha-1,4-Glucosidase Deficiency Disease . POMPE'S DISEASE . 0.52
Dysautonomia, Familial. Dominant Hereditary Sensory Neuropathy, Type III . Familial Dysautonomia . HSAN (Hereditary Sensory and Autonomic Neuropathy) Type III . HSAN 3 . HSAN III . HSAN3 . HSN-III . Hereditary Sensory Neuropathy Type 3 . Hereditary Sensory Neuropathy, Dominant, Type 3 . Hereditary Sensory Neuropathy, Dominant, Type III . Hereditary Sensory Neuropathy, Type 3, Dominant . Hereditary Sensory and Autonomic Neuropathy 3 . Neuropathy, Hereditary Sensory And Autonomic, Type III . Type 3 Hereditary Sensory Neuropathy, Dominant . Type III Hereditary Sensory Neuropathy, Dominant . Hereditary Sensory and Autonomic Neuropathy Type III . Riley Day Syndrome . Riley-Day Syndrome . HSAN Type III . Hereditary-Sensory and Autonomic Neuropathy Type III . Neuropathy, Hereditary and Autonomic, Type III . 0.49
Hereditary Sensory and Motor Neuropathy. CMT4f . Charcot-Marie-Tooth Disease, Demyelinating, Type 4f . Charcot-Marie-Tooth Disease, Type 3 . Dejerine-Sottas Neuropathy . Dejerine-Sottas Syndrome . HMSN3 . Herditary Sensory and Motor Neuropathy . Hereditary Motor and Sensory Neuropathy . Hereditary Motor and Sensory Neuropathy 3 . Hereditary Motor and Sensory Neuropathy Type III . Hypertrophic Neuropathy of Dejerine-Sottas . Charcot Marie Tooth Disease, Type 3 . Dejerine Sottas Disease . Dejerine Sottas Neuropathy . Dejerine Sottas Syndrome . Dejerine-Sottas Hypertrophic Neuropathy . Disease, Dejerine-Sottas . HMSN Type IIIs . HMSN Type VIIs . Hypertrophic Neuropathy of Dejerine Sottas . Neuropathy, Dejerine-Sottas . Syndrome, Dejerine-Sottas . Type VII, HMSN . Hereditary Motor and Sensory Neuropathies . Dejerine-Sottas Disease . HMSN 13329 . HMSN Type III . HMSN Type VII . Neuropathies, Hereditary Motor and Sensory . Hereditary, Type III, Motor and Sensory Neuropathy . Hereditary, Type VII, Motor and Sensory Neuropathy . HEREDIATARY, TYPE VII, MOTOR AND SENSORY NEUROPATHY . 0.42
