Encyclopedia of Molecular Mechanisms of Disease

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Biomedical and Life Sciences > Encyclopedia of Molecular Mechanisms of Disease

Encyclopedia of Molecular Mechanisms of Disease

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Ha Her Hm Hyperi

Hm
HMBS Deficiency → Porphyria, Acute Intermittent HMN → Neuropathies, Inherited Peripheral HMSN → Neuropathies, Inherited Peripheral HNPCC → Lynch Syndrome HNPP → Neuropathies, Inherited Peripheral HOA Hodgkin Lymphoma Hodgkin's Disease → Hodgkin Lymphoma Holt-Oram Syndrome Homocysteine: Plasma Levels and Genetic Basis Homocystinuria due to Cystathionine Beta-Synthase Deficiency Honeycomb Corneal Dystrophy → Corneal Dystrophy, Thiel-Behnke HOPP Syndrome Horton's Headache → Cluster Headache HOS → Holt-Oram Syndrome Hot Nodule → Hyperthyroidism due to Thyroid Autonomy HPA → Hyperphenylalaninemia HPD → Dopa-responsive Dystonia HPD Deficiency → Tyrosinemia Type III and Hawkinsinuria HPP → Hypophosphatasia HPS HPV → Human Papilloma Virus HPV-associated Laryngeal Cancer HRSV → Respiratory Syncytial Virus HSAN → Neuropathies, Inherited Peripheral HSAS → Hydrocephalus due to Stenosis of the Aqueduct of Sylvius HSH → Hypomagnesemia with Secondary Hypocalcemia HSP → Spastic Paraplegia, Hereditary HTE → Epilepsies, Familial Benign Myoclonic HTGL → Hepatic Triglyceride Lipase Deficiency Human Bocavirus Human Metapneumovirus Human Papilloma Virus Human RSV → Respiratory Syncytial Virus Human Transmissible Spongiform Encephalopathies Hungry Bone Syndrome Hunter Syndrome → Mucopolysaccharidoses Hunter-Thompson Type and DuPan Syndrome Huntington's Chorea → Huntington's Disease	Huntington's Disease Hurler Syndrome → Mucopolysaccharidoses HUS → Hemolytic Uremic Syndrome Hutchinson Gilford Progeria Syndrome Hyalinosis Cutis et Mucosa → Lipoid Proteinosis Hydrocele Hydrocephalus due to Stenosis of the Aqueduct of Sylvius Hydroxykynureninuria → Xanthurenic Aciduria 21-Hydroxylase Deficiency Classical Salt Wasting → Hypotension, Hereditary Hydroxymethylbilane Synthase Deficiency → Porphyria, Acute Intermittent 4-Hydroxyphenylpyruvate Dioxygenase Deficiency → Tyrosinemia Type III and Hawkinsinuria 4-Hydroxyphenylpyruvic Acid Oxidase Deficiency → Tyrosinemia Type III and Hawkinsinuria HYP Hyper IgE Syndrome Hyperaldosteronism, Primary Hyperaldosteronism, Secondary Hyperammonemia Hyperbilirubinemia Hyperbradykininism → Orthostatic Hypotensive Disorder, Familial, Streeten Type Hypercalcemia Hypercalcemia, Familial Hypocalciuric Hypercalcemia of Malignancy Hypercalciuria Hypercapnia → Acidosis, Respiratory Hypercatabolic Protein-losing Enteropathy → Intestinal Lymphangiectasia Hyperchloremic Metabolic Acidosis → Acidosis, Renal Tubular Hypercholesterolemia → Hyperlipidemia Hypercholesterolemia, Familial Hyperchylomicronemia → Lipoprotein Lipase Deficiency, Familial Hypercorticism → Cushing's Syndrome Hypercortisolism → Cushing's Syndrome Hyperdibasic Aminoaciduria Type 2 → Lysinuric Protein Intolerance Hyperekplexia, Hereditary Hyperemesis Gravidarum → Nausea and Vomiting Hypereosinophilic Syndrome → Hypereosinophilic Syndrome, Idiopathic Hypereosinophilic Syndrome, Idiopathic Hyperhomocysteinemia → Homocysteine: Plasma Levels and Genetic Basis Hyperhomocysteinemia: Genetic Basis and Arterial Thrombosis Hyperhomocysteinemia: Genetic Basis and Venous Thrombosis
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HMBS Deficiency → Porphyria, Acute Intermittent
HMN → Neuropathies, Inherited Peripheral
HMSN → Neuropathies, Inherited Peripheral
HNPCC → Lynch Syndrome
HNPP → Neuropathies, Inherited Peripheral
HOA
Hodgkin Lymphoma
Hodgkin's Disease → Hodgkin Lymphoma
Holt-Oram Syndrome
Homocysteine: Plasma Levels and Genetic Basis
Homocystinuria due to Cystathionine Beta-Synthase Deficiency
Honeycomb Corneal Dystrophy → Corneal Dystrophy, Thiel-Behnke
HOPP Syndrome
Horton's Headache → Cluster Headache
HOS → Holt-Oram Syndrome
Hot Nodule → Hyperthyroidism due to Thyroid Autonomy
HPA → Hyperphenylalaninemia
HPD → Dopa-responsive Dystonia
HPD Deficiency → Tyrosinemia Type III and Hawkinsinuria
HPP → Hypophosphatasia
HPS
HPV → Human Papilloma Virus
HPV-associated Laryngeal Cancer
HRSV → Respiratory Syncytial Virus
HSAN → Neuropathies, Inherited Peripheral
HSAS → Hydrocephalus due to Stenosis of the Aqueduct of Sylvius
HSH → Hypomagnesemia with Secondary Hypocalcemia
HSP → Spastic Paraplegia, Hereditary
HTE → Epilepsies, Familial Benign Myoclonic
HTGL → Hepatic Triglyceride Lipase Deficiency
Human Bocavirus
Human Metapneumovirus
Human Papilloma Virus
Human RSV → Respiratory Syncytial Virus
Human Transmissible Spongiform Encephalopathies
Hungry Bone Syndrome
Hunter Syndrome → Mucopolysaccharidoses
Hunter-Thompson Type and DuPan Syndrome
Huntington's Chorea → Huntington's Disease

Huntington's Disease
Hurler Syndrome → Mucopolysaccharidoses
HUS → Hemolytic Uremic Syndrome
Hutchinson Gilford Progeria Syndrome
Hyalinosis Cutis et Mucosa → Lipoid Proteinosis
Hydrocele
Hydrocephalus due to Stenosis of the Aqueduct of Sylvius
Hydroxykynureninuria → Xanthurenic Aciduria
21-Hydroxylase Deficiency Classical Salt Wasting → Hypotension, Hereditary
Hydroxymethylbilane Synthase Deficiency → Porphyria, Acute Intermittent
4-Hydroxyphenylpyruvate Dioxygenase Deficiency → Tyrosinemia Type III and Hawkinsinuria
4-Hydroxyphenylpyruvic Acid Oxidase Deficiency → Tyrosinemia Type III and Hawkinsinuria
HYP
Hyper IgE Syndrome
Hyperaldosteronism, Primary
Hyperaldosteronism, Secondary
Hyperammonemia
Hyperbilirubinemia
Hyperbradykininism → Orthostatic Hypotensive Disorder, Familial, Streeten Type
Hypercalcemia
Hypercalcemia, Familial Hypocalciuric
Hypercalcemia of Malignancy
Hypercalciuria
Hypercapnia → Acidosis, Respiratory
Hypercatabolic Protein-losing Enteropathy → Intestinal Lymphangiectasia
Hyperchloremic Metabolic Acidosis → Acidosis, Renal Tubular
Hypercholesterolemia → Hyperlipidemia
Hypercholesterolemia, Familial
Hyperchylomicronemia → Lipoprotein Lipase Deficiency, Familial
Hypercorticism → Cushing's Syndrome
Hypercortisolism → Cushing's Syndrome
Hyperdibasic Aminoaciduria Type 2 → Lysinuric Protein Intolerance
Hyperekplexia, Hereditary
Hyperemesis Gravidarum → Nausea and Vomiting
Hypereosinophilic Syndrome → Hypereosinophilic Syndrome, Idiopathic
Hypereosinophilic Syndrome, Idiopathic
Hyperhomocysteinemia → Homocysteine: Plasma Levels and Genetic Basis
Hyperhomocysteinemia: Genetic Basis and Arterial Thrombosis
Hyperhomocysteinemia: Genetic Basis and Venous Thrombosis

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