Rare Disease Index
9,491 diseasespulmonary atresia-intact ventricular septum syndrome
MeSH: C562832
pulmonary blastoma
an embryoma and malignant neoplasm of the lung
MeSH: D018202
pulmonary branch stenosis
human disease
pulmonary capillary hemangiomatosis
human disease
MeSH: C535861
pulmonary 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