HomoeOmicsDB
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Peroneal Muscular Atrophy (Axonal Type) (Hypertrophic Type)
Peroxisomal Acyl-CoA Oxidase Deficiency
Peroxisome Biogenesis Disorder 14B
Peroxisome Biogenesis Disorder 1A (Zellweger)
Peroxisome Biogenesis Disorder 2B
Peroxisome Biogenesis Disorder 3B
Peroxisome Biogenesis Disorder, Complementation Group 1
Peroxisome Biogenesis Disorder, Complementation Group A
Peroxisome Biogenesis Disorder, Complementation Group C
Peroxisome Biogenesis Disorder, Complementation Group D
Peroxisome Biogenesis Disorder, Complementation Group G
Peroxisome Biogenesis Disorder, Complementation Group H
Perry Syndrome
Perseverative Thinking
Persian Gulf Syndrome
Persistent Fetal Circulation Syndrome
Persistent Hyperplastic Primary Vitreous
Persistent Lymphocytosis
Persistent Mullerian Duct Syndrome
Persistent Oligoarticular Juvenile Idiopathic Arthritis
Persistent Polyclonal B-Cell Lymphocytosis
Persistent Pulmonary Hypertension
Persistent Vegetative State
Pertussis
Petechiae
Petit Mal Status
Peutz-Jeghers Syndrome
Peyronie Disease
Pfaundler-Hurler Syndrome
Pfeiffer Syndrome
Ph-Like Acute Lymphoblastic Leukemia
Phaeohyphomycosis
Phagocyte Bactericidal Dysfunction
Pharyngeal Carcinoma
Pharyngitis
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