HOME - Brain and Tissue Bank (Family)

Brain and Tissue Bank
University of Maryland, Baltimore
 

P


Pachydermoperiostosis

Paget's Disease

Paget's Disease of the Breast

Pallister Hall Syndrome

Pallister Killian Mosaic Syndrome

Pallister W Syndrome

Papillitis

Papillon Lefevre Syndrome

Paracoccidioidomycosis

Paramyotonia Congenita

Paraplegia, Hereditary Spastic

Parkinson's Disease

Parkinson's Disease, Idiopathic

Parry Romberg Syndrome

Pars Planitis

Parsonage Turner Syndrome

Patulous Eustachian Tube

Peeling Skin Syndrome

Pelizaeus Merzbacher Brain Sclerosis

Pemphigoid, Benign Mucosal

Pemphigus

Penta X Syndrome

Pentalogy of Cantrell

PEPCK Deficiency, Mitochondrial

Perisylvian Syndrome, Congenital Bilateral

Perniosis

Peroxisomal Disorder

Peutz Jeghers Syndrome

Peyronie Disease

Pfeiffer Syndrome Type I

Phenylketonuria

Pheochromocytoma

Phocomelia Syndrome

Phosphoglycerate Kinase Deficiency

Pick's Disease

Pierre Robin Syndrome

Pinta

Pityriasis Rubra Pilaris

Pneumonia, Eosinophilic

Pneumonia, Interstitial

POEMS Syndrome

Poland Syndrome

Polyarteritis Nodosa

Polychondritis

Polycystic Kidney Diseases

Polycystic Liver Disease

Polycythemia Vera

Polyglucosan Body Disease, Adult

Polyhydramnios

Polymyalgia Rheumatica

Polymyositis

Polyposis, Familial

Pompe Disease

Popliteal Pterygium Syndrome

Porphyria

Porphyria Cutanea Tarda

Porphyria, Acute Intermittent

Porphyria, ALA-D

Porphyria, Congenital Erythropoietic

Porphyria, Hereditary Coproporphyria

Porphyria, Variegate

Post Polio Syndrome

Posterior Urethral Valve Obstruction

Prader Willi Syndrome

Precocious Puberty

Primary Lateral Sclerosis

Progressive Osseous Heteroplasia (POH)

Progressive Supranuclear Palsy

Proteus Syndrome

Prune Belly Syndrome

Pseudo Hurler Polydystrophy

Pseudocholinesterase Deficiency

Pseudohypoparathyroidism

Pseudomyxoma Peritonei

Pseudotumor Cerebri

Pseudoxanthoma Elasticum (PXE)

Pterygium Syndrome, Multiple

Pulmonary Alveolar Proteinosis

Pulmonary Hypertension, Primary

Pulmonary Hypertension, Secondary

Pure Red Cell Aplasia, Acquired

Pyknodysostosis

Pyoderma Gangrenosum

Pyruvate Carboxylase Deficiency

Pyruvate Dehydrogenase Deficiency

Pyruvate Kinase Deficiency