Disease Index - ty

TYK2 Deficiency
Tylosis
Tylosis with esophageal cancer
Tympanic Calcification
Tympanic Membrane Perforation
Tympanic Membrane Rupture
Tympanoscleroses
Tympanosclerosis
Tympanosclerosis, Intratympanic
Type 1 AIP
type 1 Amaurosis congenita of Leber
type 1 Atelosteogenesis
Type 1 Autoimmune Pancreatitis
type 1 Autoimmune polyendocrinopathy syndrome
Type 1 Benign Adult Familial Myoclonic Epilepsy
Type 1 Bipolar Disorder
type 1 Corneal dystrophy of Bowman layer
Type 1 Craniosynostoses
Type 1 Craniosynostosis
type 1 Dentin dysplasia
Type 1 Diabetes
Type 1 Diabetes Mellitus
Type 1 Duane Retraction Syndrome
Type 1 Episodic Ataxia
type 1 familial Hypocalciuric hypercalcemia
Type 1 Familial Parkinson Disease
Type 1 FFDD
Type 1 Gaucher Disease
Type 1 Generalized Epilepsy With Febrile Seizures Plus
Type 1 Hyper-IgM Immunodeficiency Syndrome
Type 1 Kenny-Caffey syndrome
Type 1 Lissencephalies
Type 1 Lissencephaly
Type 1 Maturity-Onset Diabetes of the Young
type 1 Microcephalic osteodysplastic primordial dwarfism
Type 1 nephronophthisis
Type 1 Neurofibromatosis
Type 1 Pachyonychia Congenita
type 1 Pena Shokeir syndrome
type 1 Polycystic kidney disease
Type 1 Porencephaly
Type 1 Spherocytosis
Type 1 Spinocerebellar Ataxia
type 1 Stickler syndrome
Type 1 tracheomalacia
Type 1 von Willebrand Disease
Type 1, Fucosidosis
Type 1, Lissencephaly
Type 1, Neurofibromatosis
Type 1, Pseudohypoaldosteronism
Type 1.5 Diabetes
Type 1.5 Diabetes Mellitus
type 1A Osteogenesis imperfecta
Type 1A Vitamin D Hydroxylation-Deficient Rickets
type 1B Limb-girdle muscular dystrophy
type 1B Usher syndrome
Type 1B Vitamin D Hydroxylation-Deficient Rickets
Type 1C Charcot-Marie-Tooth disease
Type 1C Limb-Girdle Muscular Dystrophy
type 1C Usher syndrome
Type 1D Charcot-Marie-Tooth disease
Type 1D Limb-Girdle Muscular Dystrophy
type 1D Usher syndrome
Type 1E Charcot-Marie-Tooth disease
Type 1e Demyelinating Charcot-Marie-Tooth Disease
Type 1E Limb-Girdle Muscular Dystrophy
Type 1F Charcot-Marie-Tooth disease
Type 1F Limb-Girdle Muscular Dystrophy
type 1F Usher syndrome
Type 1G Limb-Girdle Muscular Dystrophy
Type 1s, Fucosidosis
Type 1s, Lissencephaly
Type 2 AIP
type 2 alpha 1 Collagenopathy
type 2 Amaurosis congenita of Leber
Type 2 Autoimmune Pancreatitis
Type 2 Benign Adult Familial Myoclonic Epilepsy
Type 2 Bipolar Disorder
Type 2 Combined Deficiency Of Vitamin K-Dependent Clotting Factors
Type 2 Craniosynostosis
type 2 Crigler Najjar syndrome
Type 2 Diabetes
Type 2 Diabetes Mellitus
Type 2 Duane Retraction Syndrome
Type 2 Episodic Ataxia
Type 2 FFDD
Type 2 Gaucher Disease
Type 2 Generalized Epilepsy With Febrile Seizures Plus
Type 2 Hdl Deficiency
type 2 Hemochromatosis
Type 2 Histiocytoses
Type 2 Histiocytosis
Type 2 hyperprolinemia
Type 2 Hypokalemic Periodic Paralysis
type 2 Kenny-Caffey syndrome
type 2 Lamellar ichthyosis
Type 2 lamellar ichthyosis
type 2 Maple syrup urine disease
Type 2 Maturity-Onset Diabetes of the Young
Type 2 Neurofibromatoses
Type 2 Neurofibromatosis
type 2 Oto-palato-digital syndrome
Type 2 Pachyonychia Congenita
Type 2 Punctate PPK
type 2 Rhizomelic chondrodysplasia punctata
Type 2 rhizomelic chondrodysplasia punctata
Type 2 Spinocerebellar Ataxia
type 2 Stickler syndrome
type 2 Syndactyly
Type 2 Tyrosinemia
Type 2 Tyrosinemias
Type 2 von Willebrand Disease
Type 2, 3-Methylglutaconicaciduria
Type 2, Hyperlipoproteinemia
Type 2, MGA
Type 2A Charcot-Marie-Tooth disease
type 2A Osteogenesis imperfecta
type 2A Usher syndrome
Type 2A Vitamin D-Dependent Rickets
Type 2A von Willebrand Disease
Type 2a1 Axonal Charcot-Marie-Tooth Disease
Type 2A2 Axonal Charcot-Marie-Tooth Disease
Type 2B Charcot-Marie-Tooth disease
type 2B Limb-girdle muscular dystrophy
type 2B Osteogenesis imperfecta
Type 2B von Willebrand Disease
Type 2B1 Charcot-Marie-Tooth disease
Type 2B2 Charcot-Marie-Tooth disease
type 2C Congenital disorder of glycosylation
type 2C Limb-girdle muscular dystrophy
Type 2D Charcot-Marie-Tooth disease
Type 2E Charcot-Marie-Tooth disease
type 2E Limb-girdle muscular dystrophy
Type 2F Charcot-Marie-Tooth disease
Type 2G Limb-Girdle Muscular Dystrophy
Type 2I Charcot-Marie-Tooth disease
Type 2I Limb-Girdle Muscular Dystrophy
Type 2J Charcot-Marie-Tooth disease
Type 2J Limb-Girdle Muscular Dystrophy
Type 2K Charcot-Marie-Tooth disease
Type 2L Limb-Girdle Muscular Dystrophy
Type 2M Limb-Girdle Muscular Dystrophy
Type 2M von Willebrand Disease
Type 2N von Willebrand Disease
Type 2s, MGA
Type 3 (Adult) GM1 Gangliosidosis
type 3 Bartter syndrome
Type 3 Congenital Generalized Lipodystrophy
Type 3 Duane Retraction Syndrome
type 3 familial Alzheimer disease
Type 3 FFDD
Type 3 Gaucher Disease
type 3 Hemochromatosis
Type 3 Hereditary Sensory Neuropathy, Dominant
type 3 Lamellar ichthyosis
Type 3 lamellar ichthyosis
Type 3 Maturity-Onset Diabetes of the Young
type 3 Osteogenesis imperfecta
type 3 Rhizomelic chondrodysplasia punctata
Type 3 Spinocerebellar Ataxia
type 3 Stickler syndrome
Type 3 von Willebrand Disease
Type 3 Von Willebrand's Disease
Type 3 VWD
Type 3, Neurofibromatosis
Type 4 Episodic Ataxia
Type 4 FFDD
Type 4 FFDDs
type 4 Hemochromatosis
Type 4 Maturity-Onset Diabetes of the Young
Type 4 Noninsulin-Dependent Diabetes Mellitus
Type 4 Spherocytosis
Type 4 Spinocerebellar Ataxia
type 4 Waardenburg syndrome
Type 4A Bartter Syndrome
Type 4A Charcot-Marie-Tooth disease
Type 4B1 Charcot-Marie-Tooth disease
Type 4B2 Charcot-Marie-Tooth disease
Type 4C Charcot-Marie-Tooth disease
Type 4E Charcot-Marie-Tooth disease
Type 4H Charcot-Marie-Tooth Disease
Type 4j Charcot-Marie-Tooth Disease
type 5 Amaurosis congenita of Leber
type 5 congenital Adrenal hyperplasia
Type 5 Spherocytosis
Type 5 Spinocerebellar Ataxia
type 6 Amyotrophic lateral sclerosis
Type 6 Episodic Ataxia
Type 6 MODY
type 6 Osteogenesis imperfecta
Type 6 Spinocerebellar Ataxia
Type 6, Mucopolysaccharidosis
Type 7 Maturity-Onset Diabetes of the Young
Type 7 Spinocerebellar Ataxia
Type 8 Maturity-Onset Diabetes of the Young with Exocrine Dysfunction
type 9 Amaurosis congenita of Leber
Type 9 Maturity-Onset Diabetes Of The Young
Type A Cockayne Syndrome
Type A Cystinuria
Type A Niemann Pick Disease
Type A Niemann-Pick Disease
Type A2 Postaxial Polydactyly
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 B1 Brachydactyly
Type C Cockayne Syndrome
Type C Lethargic Encephalitis
Type C Niemann-Pick Disease
type C2 Niemann-Pick disease
Type D Brachydactyly
Type E Brachydactyly
Type F Niemann-Pick Disease
Type G-Cockayne Syndrome Xeroderma Pigmentosum
Type I 3-Methylglutaconic Aciduria
Type I Acrocephalosyndactylies
Type I Acrocephalosyndactyly
Type I Arnold Chiari Malformation
Type I Arnold-Chiari Malformation
Type I Ataxia with Lactic Acidosis
Type I Bare Lymphocyte Syndrome
Type I Canavan Disease
Type I Citrullinemia
Type I Citrullinemias
Type I Cockayne Syndrome
Type I Complex Regional Pain Syndrome
Type I Congenital Dyserythropoietic Anemia
Type I Familial Amyloid Polyneuropathy
Type I familial incomplete male pseudohermaphroditism
Type I GM1-Gangliosidoses
Type I GM1-Gangliosidosis
Type I GM2-Gangliosidosis
Type I Hyperlipoproteinemia
Type I Hyperlipoproteinemias
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 Plasminogen Deficiency
Type I Pseudohypoaldosteronism
Type I Renal Tubular Acidosis
Type I Schindler Disease
Type I Spinal Muscular Atrophy
Type I Syndactyly
Type I Thanatophoric Dysplasia
Type I Tyrosinemia
Type I Tyrosinemias
Type I von Willebrand Disease
Type I Xanthinuria
Type I, CRPS
Type I, HSAN
Type I, HSN
Type I, Neurofibromatosis
Type I, Pseudohypoaldosteronism
Type IA Autoimmune Lymphoproliferative Syndrome
Type Ia Hyperlipoproteinemia
Type Ia Hyperlipoproteinemias
Type Ia Pseudohypoparathyroidism
Type Ia Pseudohypoparathyroidisms
Type Ib Hyperlipoproteinemia
Type Ib Hyperlipoproteinemias
Type IB Isolated Growth Hormone Deficiency
Type Ib Pseudohypoparathyroidism
Type Ib Pseudohypoparathyroidisms
Type Ib Usher Syndrome
Type IC Usher Syndrome
Type Ih, Mucopolysaccharidosis
Type Ihs, Mucopolysaccharidosis
Type II 3beta-Hydroxysteroid Dehydrogenase Deficiency
Type II Acrocephalosyndactylies
Type II Acrocephalosyndactyly
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 Distal Hereditary Motor Neuropathy
Type II Familial Amyloid Polyneuropathy
Type II GM1-Gangliosidoses
Type II GM1-Gangliosidosis
Type II GM2-Gangliosidoses
Type II GM2-Gangliosidosis
Type II Hyperlipoproteinemia
Type II Hyperlipoproteinemias
Type II Isolated Growth Hormone Deficiency
Type II Lattice Corneal Dystrophy
Type II Machado Joseph Disease
Type II Machado-Joseph Disease
Type II Macular Corneal Dystrophy
Type II Metatropic Dwarfism
Type II Microcephalic Osteodysplastic Primordial Dwarfism
Type II MPGN
Type II MPGNs
Type II Mucolipidoses
Type II Mucolipidosis
Type II Neurofibromatoses
Type II Neurofibromatosis
Type II Nonketotic Hyperglycinemia
Type II Progressive Familial Heart Block
Type II Properdin Deficiency
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 Xanthinuria
Type II, Glycogenosis
Type II, MGA
Type II, Pseudohypoaldosteronism
Type IIa Hyperlipoproteinemia
Type IIa Hyperlipoproteinemias
Type IIA von Willebrand Disease
Type IIB Autosomal Recessive Cutis Laxa
Type IIB Congenital Disorder Of Glycosylation
Type IIB Hereditary Sensory And Autonomic Neuropathy
Type IIB von Willebrand Disease
Type IIC Hereditary Motor And Sensory Neuropathy
Type IIF Congenital Disorder Of Glycosylation
Type III Acrocephalosyndactyly
Type III Amelogenesis Imperfecta
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 GM1-Gangliosidoses
Type III GM1-Gangliosidosis
Type III Hereditary Sensory Neuropathy, Dominant
Type III Hyperlipoproteinemia
Type III Hyperlipoproteinemias
Type III Hypersensitivities
Type III Hypersensitivity
Type III Leukocyte Adhesion Deficiency
Type III Machado Joseph Disease
Type III Machado-Joseph Disease
Type III Mucolipidoses
Type III Mucolipidosis
Type III Nonketotic Hyperglycinemia
Type III Properdin Deficiency
Type III Spinal Muscular Atrophy
Type III Tyrosinemia
Type III Tyrosinemias
Type IIIb Gaucher Disease
Type Iiic Gaucher Disease
Type IIID Congenital Disorder Of Glycosylation
Type IIM von Willebrand Disease
Type IIN von Willebrand Disease
Type IIs, Glycogenosis
Type IIs, MGA
Type IIs, Pseudohypoaldosteronism
Type Is, Pseudohypoaldosteronism
Type IV Arnold Chiari Malformation
Type IV Arnold-Chiari Malformation
Type IV Ehlers Danlos Syndrome
Type IV Ehlers-Danlos Syndrome
Type IV Familial Amyloid Polyneuropathy
Type IV Glycogenoses
Type IV Glycogenosis
Type IV Hyperlipoproteinemia
Type IV Hyperlipoproteinemias
Type IV Hypersensitivities
Type IV Hypersensitivity
Type IV Machado Joseph Disease
Type IV Machado-Joseph Disease
Type IV Mucolipidoses
Type IV Mucolipidosis
Type IV Oculocutaneous Albinism
Type IV Osteogenesis Imperfecta
Type IV Renal Tubular Acidosis
Type IV Spinal Muscular Atrophy
Type IV, HSAN
Type IV, Hyperlipoproteinemia
Type IV, Mucopolysaccharidosis
Type IVs, Mucopolysaccharidosis
Type IX Osteogenesis Imperfecta
Type IXD Glycogen Storage Disease
Type Microcytemia, beta
Type Microcytemias, beta
Type Porphyria, Swedish
Type Porphyrias, Swedish
Type Thalassemia, beta
Type Thalassemias, beta
Type Thrombocytopenia, Paris-Trousseau
Type Tyrosinoses, Oculocutaneous
Type Tyrosinosis, Oculocutaneous
Type V 3-Methylglutaconic Aciduria
Type V Acrocephalosyndactylies
Type V Acrocephalosyndactyly
Type V Distal Hereditary Motor Neuronopathy
Type V Familial Amyloid Polyneuropathy
Type V Hereditary Motor and Sensory Neuropathy
Type V Hyperlipidemia
Type V Hyperlipidemias
Type V Hyperlipoproteinemia
Type V Hyperlipoproteinemias
Type V Osteogenesis Imperfecta
type v Syndactyly
Type V, HMSN
Type VI Familial Amyloid Polyneuropathy
Type VI, Glycogenosis
Type VI, Mucopolysaccharidosis
Type VII, HMSN
Type VII, Mucopolysaccharidosis
Type Viib Distal Hereditary Motor Neuronopathy
Type VIII Ehlers-Danlos Syndrome
type VIII Osteogenesis imperfecta
Type VIIs, Mucopolysaccharidosis
Typhlitis
Typhlitis, Neutropenic
Typhoid
Typhoid Fever
Typhoid Fevers
Typhoids
Typhus
Typhus Infection, Murine
Typhus Infections, Murine
Typhus, Abdominal
Typhus, Endemic
Typhus, Endemic Flea Borne
Typhus, Endemic Flea-Borne
Typhus, Epidemic
Typhus, Epidemic Louse Borne
Typhus, Epidemic Louse-Borne
Typhus, Louse-Borne
Typhus, Murine
Typhus, Queensland Tick
Typhus, Sao Paulo
Typhus, Scrub
Typical Aura without Headache
Typical Teratoid Rhabdoid Tumor
Typical Teratoma Rhabdoid Tumor
Typical Teratoma-Rhabdoid Tumor
Typus Degenerativus Amstelodamensis
Tyrosinase-Negative Albinism
Tyrosinase-Positive Albinism
Tyrosinase-positive oculocutaneous albinism
Tyrosine Aminotransferase Deficiency
Tyrosine Hydroxylase Deficiency
Tyrosine Kinase 2 Deficiency
Tyrosine Transaminase Deficiency
Tyrosine Transaminase Deficiency Disease
Tyrosinemia
Tyrosinemia Type 1
Tyrosinemia Type 1s
Tyrosinemia, Hepatorenal
Tyrosinemia, Hereditary
Tyrosinemia, Type 2
Tyrosinemia, Type I
Tyrosinemia, Type II
Tyrosinemia, Type III
Tyrosinemias
Tyrosinemias, Hepatorenal
Tyrosinemias, Hereditary
Tyrosinemias, Type 2
Tyrosinemias, Type I
Tyrosinemias, Type II
Tyrosinemias, Type III
Tyrosinoses, Oculocutaneous Type
Tyrosinosis
Tyrosinosis, Oculocutaneous Type