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Biomedical and Life Sciences
> Encyclopedia of Molecular Mechanisms of Disease
Encyclopedia of Molecular Mechanisms of Disease
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P d
Pb
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P d
5p Deletion Syndrome
8p Inverted Duplication
→
Inv Dup Del (8p)
P. Jiroveci Pneumonia
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Pneumocystis Pneumonia
8p Mirror Duplication
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Inv Dup Del (8p)
5p Monosomy
9p Monosomy
→
Deletion 9p Syndrome
4p Syndrome
→
Wolf-Hirschhorn Syndrome
5p Syndrome
9p Syndrome
→
Deletion 9p Syndrome
PACD
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Corneal Dystrophy, Posterior Amorphous
Pachydermoperiostosis
Pachyonychia Congenita
Pachyonychia Congenita Type I
→
Pachyonychia Congenita
PACNS
→
Vasculitis, Cerebral Forms
PAD
→
Peripheral Artery Disease
PAF
Paget's Disease of Bone
PAH1
Painful Plantar Warts or Vegetative Warts
→
Human Papilloma Virus
PAIS
→
Androgen Insensitivity Syndrome
PA/IVS
→
Pulmonary Atresia
PAIVS
→
Pulmonary Atresia
Pallister-Killian Syndrome
Palmitoylcarnitine Transferase
Palmoplantar Keratoderma
Palmoplantar Keratoderma Vörner-Unna-Thost
PAN
Pancreas Annulare
→
Annular Pancreas
Pancreatic Adenocarcinoma
→
Pancreatic Cancer
Pancreatic Cancer
Pancreatic Carcinoma
→
Pancreatic Cancer
Pancreatic ß-cell Tumor
→
Insulinoma
Pancreatic Cholera Syndrome
→
VIPoma
Pancreatic Insufficiency and Bone Marrow Dysfunction
→
Shwachman Diamond Syndrome
Pancreatic Nesidioblastosis
→
Persistent Hyperinsulinemic Hypoglycemia
Pancreatitis, Acute
Pancreatitis, Autoimmune
Pancreatitis, Chronic
Pancreatitis, Hereditary
Panniculitis
Panniculitis at α-1 Antitrypsin Deficiency
Panniculitis Mesenterica
→
Mesenteric Lipodystrophy
PAP
→
Pulmonary Alveolar Proteinosis
Papillary Duct Ectasia
→
Medullary Sponge Kidney
Papillary Thyroid Cancer
→
Thyroid Cancer
Papillon-Léage
→
Brachydactyly: Oro-facio-digital Syndrome Type I
Papillon-Lefèvre Syndrome
Paraganglioma
Paralyses, Periodic
→
Periodic Paralyses, Familial
Paramyoclonus Multiplex Friedreich
→
Myoclonus-Dystonia
Paramyotonia
→
Myotonia and Paramyotonia
Paramyotonia Congenita (Eulenburg, PC)
→
Myotonia and Paramyotonia
Paraneoplastic
→
Lambert Eaton Myasthenic Syndrome
Paraneoplastic Syndromes
Parasternal Chondrodynia
→
Tietze's Syndrome
Parathyroid Hormone and Related Peptides
Parenchymatous Cholestasis
→
Jaundice, Hepatocellular
Parkinson's Disease
Paroxismal Nocturnal Hemoglobinuria
Paroxysmal Cold Hemoglobinuria
→
Anemia, Hemolytic Autoimmune
Paroxysmal Dyskinesias
Paroxysmal Dystonic Choreoathetosis
→
Paroxysmal Dyskinesias
Paroxysmal Supraventricular Tachycardia
→
Tachycardia, Supraventricular
Pars Planitis
→
Uveitis
Partial 11q Monosomy Syndrome
→
Jacobsen Syndrome
Partial Albinism
→
Piebaldism
Partial Androgen Insensitivity Syndrome
→
Androgen Insensitivity Syndrome
Partial Epilepsies of Childhood
→
Epilepsy, Benign Childhood with Centrotemporal Spikes and other Idiopathic Partial Epilepsies of Childhood
Partial Persistent Truncus Arteriosus
→
Aortopulmonary Septal Defects
Partial Tetrasomy 15(pter-q13)
Partial Tetrasomy or Trisomy (22pter-22q11)
→
Cat Eye Syndrome
Patau Syndrome
→
Trisomy 13
Patent Ductus Arteriosus
Patent Foramen Ovale
Patent Omphalomesenteric Duct
Patent Vitelline Duct
→
Patent Omphalomesenteric Duct
Pathological Gambling
Pauci-immune Glomerulonephritis
→
Glomerulonephritis, Crescentic
PA-VSD
→
Pulmonary Atresia
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