HomoeOmicsDB
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Diseases
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Peroxisome Biogenesis Disorder, Complementation Group A
Peroxisome Biogenesis Disorder, Complementation Group D
Peroxisome Biogenesis Disorder, Complementation Group H
Perry Syndrome
Persistent Fetal Circulation Syndrome
Persistent Hyperplastic Primary Vitreous
Persistent Lymphocytosis
Persistent Polyclonal B-Cell Lymphocytosis
Persistent Pulmonary Hypertension
Persistent Vegetative State
Pertussis
Petechiae
Petit Mal Status
Petty Laxova Wiedemann Syndrome
Peutz-Jeghers Syndrome
Peyronie Disease
Pfeiffer Syndrome
Ph-Like Acute Lymphoblastic Leukemia
Pharyngeal Carcinoma
Pharyngitis
Pheochromocytoma
Pheochromocytoma, Malignant
Philadelphia Chromosome Positive Chronic Myelogenous Leukemia
Phobia, Social
Phobic Anxiety Disorder
Phonophobia
Phosphate Diabetes
Photoparoxysmal Response 1
Photoreceptor Degeneration
Phototoxicity
Phrynoderma
Phyllodes Tumor
Physical Addiction
Pick Disease Of The Brain
Piebaldism
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