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Disease Index - ty

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Tylosis
Tympanic Membrane Perforation
Tympanic Membrane Rupture
Type 1 Diabetes Mellitus
Type 1 Duane Retraction Syndrome
Type 1 Gaucher Disease
Type 1 Hyper-IgM Immunodeficiency Syndrome
Type 1 Lissencephalies
Type 1 Lissencephaly
Type 1 Neurofibromatosis
Type 1 Pachyonychia Congenita
Type 1 Spinocerebellar Ataxia
Type 1 von Willebrand Disease
Type 1, Citrullinemia
Type 1, Fucosidosis
Type 1, Mucolipidosis
Type 1, Neurofibromatosis
Type 1, Pseudohypoaldosteronism
Type 1s, Fucosidosis
Type 1s, Mucolipidosis
Type 1s, Pseudohypoaldosteronism
Type 2 Diabetes Mellitus
Type 2 Duane Retraction Syndrome
Type 2 Gaucher Disease
Type 2 Neurofibromatoses
Type 2 Neurofibromatosis
Type 2 Pachyonychia Congenita
Type 2 Spinocerebellar Ataxia
Type 2 von Willebrand Disease
type 2, 3-methylglutaconicaciduria
Type 2, Hyperlipoproteinemia
Type 2, Mucopolysaccharidosis
Type 2, Pseudohypoaldosteronism
Type 2A von Willebrand Disease
Type 2B von Willebrand Disease
Type 2M von Willebrand Disease
Type 2N von Willebrand Disease
type 2s, 3-methylglutaconicaciduria
Type 2s, Hyperlipoproteinemia
Type 2s, Mucopolysaccharidosis
Type 2s, Pseudohypoaldosteronism
Type 3 (Adult) GM1 Gangliosidosis
Type 3 Duane Retraction Syndrome
Type 3 Gaucher Disease
Type 3 Hereditary Sensory Neuropathy, Dominant
Type 3 Spinocerebellar Ataxia
Type 3 von Willebrand Disease
Type 3 Von Willebrand's Disease
Type 3 VWD
Type 3, Neurofibromatosis
Type 4 Spinocerebellar Ataxia
Type 5 Spinocerebellar Ataxia
Type 6 Spinocerebellar Ataxia
Type 6, Mucopolysaccharidosis
Type 6s, Mucopolysaccharidosis
Type 7 Spinocerebellar Ataxia
Type A Cockayne Syndrome
Type A Niemann Pick Disease
Type A Niemann-Pick Disease
Type Acroosteolysis, Giaccai
Type B Cockayne Syndrome
Type B Haemophilus influenzae Meningitis
Type B Hemophilus influenzae Meningitis
Type B Niemann Pick Disease
Type B Niemann-Pick Disease
Type C Cockayne Syndrome
Type C Lethargic Encephalitis
Type C Niemann-Pick Disease
Type I Arnold Chiari Malformation
Type I Arnold-Chiari Malformation
Type I Canavan Disease
Type I Cockayne Syndrome
Type I Complex Regional Pain Syndrome
Type I Congenital Dyserythropoietic Anemia
Type I Familial Amyloid Polyneuropathy
Type I Hypersensitivities
Type I Hypersensitivity
Type I Hypertyrosinemia
Type I Hypertyrosinemias
Type I Machado Joseph Disease
Type I Machado-Joseph Disease
Type I Mucolipidoses
Type I Mucolipidosis
Type I Neurofibromatoses
Type I Nonketotic Hyperglycinemia
Type I Pseudohypoaldosteronism
Type I Pseudohypoaldosteronisms
Type I Renal Tubular Acidosis
Type I Spinal Muscular Atrophy
Type I Tyrosinemia
Type I Tyrosinemias
Type I von Willebrand Disease
Type I, CPRS
Type I, HSAN
Type I, HSN
Type I, Neurofibromatosis
Type II Arnold Chiari Malformation
Type II Arnold-Chiari Malformation
Type II Ataxia with Lactic Acidosis
Type II Canavan Disease
Type II Cockayne Syndrome
Type II Complex Regional Pain Syndrome
Type II Familial Amyloid Polyneuropathy
Type II Machado Joseph Disease
Type II Machado-Joseph Disease
Type II Mucolipidoses
Type II Mucolipidosis
Type II Neurofibromatoses
Type II Neurofibromatosis
Type II Nonketotic Hyperglycinemia
Type II Pseudohypoaldosteronism
Type II Pseudohypoaldosteronisms
Type II Renal Tubular Acidosis
Type II Spinal Muscular Atrophy
Type II Tyrosinemia
Type II Tyrosinemias
Type II von Willebrand Disease
type II, 3-methylglutaconicaciduria
Type II, Glycogenosis
type II, MGA
Type IIA von Willebrand Disease
Type IIB von Willebrand Disease
Type III Arnold Chiari Malformation
Type III Arnold-Chiari Malformation
Type III Canavan Disease
Type III Cockayne Syndrome
Type III Familial Amyloid Polyneuropathy
Type III Hereditary Sensory Neuropathy, Dominant
Type III Hypersensitivities
Type III Hypersensitivity
Type III Machado Joseph Disease
Type III Machado-Joseph Disease
Type III Mucolipidoses
Type III Mucolipidosis
Type III Nonketotic Hyperglycinemia
Type III Spinal Muscular Atrophy
Type III Tyrosinemia
Type III Tyrosinemias
Type IIM von Willebrand Disease
Type IIN von Willebrand Disease
type IIs, 3-methylglutaconicaciduria
Type IIs, Glycogenosis
Type IIs, HMSN
type IIs, MGA
Type Is, CPRS
Type IV Arnold Chiari Malformation
Type IV Arnold-Chiari Malformation
Type IV Familial Amyloid Polyneuropathy
Type IV Glycogenoses
Type IV Glycogenosis
Type IV Hypersensitivities
Type IV Hypersensitivity
Type IV Machado Joseph Disease
Type IV Machado-Joseph Disease
Type IV Mucolipidoses
Type IV Mucolipidosis
Type IV Renal Tubular Acidosis
Type IV, HSAN
Type IV, Hyperlipoproteinemia
Type V Familial Amyloid Polyneuropathy
Type V Hereditary Motor and Sensory Neuropathy
Type V, HMSN
Type V, HSAN
Type VI Familial Amyloid Polyneuropathy
Type VI, Glycogenosis
Type VII, HMSN
Typhlitis
Typhlitis, Neutropenic
Typhoid
Typhoid Fever
Typhoid Fevers
Typhoids
Typhus
Typhus, Abdominal
Typhus, Endemic
Typhus, Endemic Flea Borne
Typhus, Endemic Flea-Borne
Typhus, Epidemic
Typhus, Epidemic Louse Borne
Typhus, Epidemic Louse-Borne
Typhus, Murine
Typhus, Sao Paulo
Typhus, Scrub
Typical Aura without Headache
Typus Degenerativus Amstelodamensis
Tyrosinase-Negative Albinism
Tyrosinase-Positive Albinism
Tyrosine Transaminase Deficiency Disease
Tyrosinemia
Tyrosinemia, Hereditary
Tyrosinemia, Type I
Tyrosinemia, Type II
Tyrosinemia, Type III
Tyrosinemias
Tyrosinemias, Hereditary
Tyrosinemias, Type I
Tyrosinemias, Type II
Tyrosinemias, Type III

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