Disease Index
9,486 diseasespulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome
pulmonary hemosiderosis
human disease
MeSH: D000097545
pulmonary hypertension
medical condition
MeSH: D006976
pulmonary hypertension owing to lung disease and/or hypoxia
human disease
pulmonary hypertension with unclear multifactorial mechanism
human disease
pulmonary hypertension, primary, 1
human disease
pulmonary hypoplasia
congenital disorder of respiratory system
ICD: Q33.6
pulmonary interstitial glycogenosis
Pulmonary interstitial glycogenosis (PIG) is a rare non-lethal pediatric form of interstitial lung disease (ILD, see this term)
pulmonary nodular lymphoid hyperplasia
Pulmonary nodular lymphoid hyperplasia (PNHL) is a reactive lymphoid proliferation manifesting as solitary or multiple nodules in the lung
pulmonary sequestration
congenital disorder of respiratory system
ICD: Q33.2MeSH: D001998
pulmonary valve agenesis
congenital abnormality
pulmonary valve agenesis-tetralogy of fallot-absence of ductus arteriosus syndrome
human disease
pulmonary valve agenesis-ventricular septal defect-persistent ductus arteriosus syndrome
human disease
pulmonary valve stenosis
Human disease
ICD: I37.0MeSH: D011666
pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis
disease
pulmonary venoocclusive disease
Human disease
MeSH: D011668
punctate palmoplantar keratoderma
palmoplantar keratosis characterized by keratoses with a "raindrop" pattern on the palmoplantar surface, skin lesions which may involve the whole of the palmoplantar surface, or may be more restricted in their distribution
ICD: Q82.8
punctate palmoplantar keratoderma type 1
punctate palmoplantar keratoderma type II
human disease
punctate palmoplantar keratoderma type III
Human disease
MeSH: C535653
PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome
human disease
pure autonomic failure
neurodegenerative disease that affects the sympathetic branch of the autonomous nervous system and that manifests with orthostatic hypotension
MeSH: D054970
pure hair-nail type ectodermal dysplasia
human disease
MeSH: C566592
pure hereditary spastic paraplegia
human disease
Pure mitochondrial myopathy
pure or complex autosomal dominant spastic paraplegia
human disease
pure or complex autosomal recessive spastic paraplegia
human disease
pure or complex hereditary spastic paraplegia
human disease
pure or complex X-linked spastic paraplegia
human disease
pure red-cell aplasia
human disease
ICD: D60MeSH: D012010