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Ontology Browser

Term:
pulmonary alveolar microlithiasis (DOID:12117)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
calcinosis +     
genetic disease +     
lung disease +     
46,XX Sex Reversal with Dysgenesis of Kidneys, Adrenals, and Lungs  
acute chest syndrome  
Adrenocortical Hypofunction, Chronic Primary Congenital 
adrenocorticotropic hormone deficiency  
adult respiratory distress syndrome  
advanced sleep phase syndrome 1  
advanced sleep phase syndrome 2  
advanced sleep phase syndrome 3  
age related macular degeneration 8  
Alagille syndrome  
alpha 1-antitrypsin deficiency  
Alpha-2-Deficient Collagen Disease 
Alpha-2-Macroglobulin Deficiency  
alveolar echinococcosis 
Alzheimer's disease 18  
Aortic Valve, Calcification of  
AQUAPORIN 1 DEFICIENCY  
ataxia telangiectasia +   
ataxic cerebral palsy 
atrial heart septal defect 3  
atrial heart septal defect 4  
autoimmune lymphoproliferative syndrome +   
Bacterial Lung Diseases +   
Baraitser Brett Piesowicz Syndrome 
basal ganglia calcification +   
Berry Aneurysm, Cirrhosis, Pulmonary Emphysema, and Cerebral Calcification 
brachydactyly type A1B 
brachydactyly type A1C  
brachydactyly type A1D  
brachydactyly type B1  
brachydactyly type B2  
brachydactyly type E1  
brachydactyly type E2  
CADASIL +   
CAKUT2  
Calcific Aortic Disease with Immunologic Abnormalities, Familial 
Calcification of Joints and Arteries +   
calciphylaxis 
capillariasis 
cataract 1 multiple types  
cataract 10 multiple types  
cataract 11 multiple types +   
cataract 12 multiple types  
cataract 13 with adult i phenotype  
cataract 14 multiple types  
cataract 15 multiple types  
cataract 16 multiple types  
cataract 18  
cataract 2 multiple types  
cataract 20 multiple types  
cataract 21 multiple types  
cataract 23  
cataract 24 
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
cataract 29 
cataract 3 multiple types  
cataract 30  
cataract 31 multiple types  
cataract 33  
cataract 36  
cataract 37 
cataract 38  
cataract 41  
cataract 42  
cataract 43  
cataract 44  
cataract 45  
cataract 46 juvenile-onset  
Cataract 48  
cataract 5 multiple types  
cataract 7  
cataract 8 multiple types 
cataract 9 multiple types  
Cenani-Lenz syndactyly syndrome  
Cerebroretinal Microangiopathy with Calcifications and Cysts +   
CHARGE syndrome  
cherubism +   
CHOPS SYNDROME  
Choroid Plexus Calcification with Mental Retardation 
chromosomal disease +   
chronic granulomatous disease +   
Cole Disease  
complement factor I deficiency  
complex cortical dysplasia with other brain malformations 1  
complex cortical dysplasia with other brain malformations 2  
complex cortical dysplasia with other brain malformations 3  
complex cortical dysplasia with other brain malformations 4  
complex cortical dysplasia with other brain malformations 5  
complex cortical dysplasia with other brain malformations 6  
complex cortical dysplasia with other brain malformations 7  
congenital diarrhea +   
congenital hemolytic anemia +   
Congenital Hepatic Fibrosis  
congenital hypoplastic anemia +   
congenital muscular dystrophy +   
congenital myasthenic syndrome +   
Congenital Pain Insensitivity +   
corneal opacification and other ocular anomalies +   
CREST syndrome  
Cystic Adenomatoid Malformation of Lung, Congenital 
Cystic Disease of Lung 
cystic echinococcosis  
cystic fibrosis +   
desquamative interstitial pneumonia  
diffuse idiopathic skeletal hyperostosis +   
dirofilariasis 
Dwarfism +   
Encephalopathy with Intracranial Calcification, Growth Hormone Deficiency, Microcephaly, and Retinal Degeneration 
Epilepsy, Occipital Calcifications 
Facial Dysmorphism, Selective Tooth Agenesis, and Choroid Calcification 
Familial Cirrhosis +   
Familial Dysalbuminemic Hyperthyroxinemia  
Familial Hemophagocytic Lymphohistiocytoses +   
familial hypertrophic cardiomyopathy +   
Familial Lipochrome Histiocytosis 
Familial Mixed Cryoglobulinemia  
Familial Temporal Epilepsy +   
Fatal Fetal Cardiomyopathy due to Myocardial Calcification 
FTDALS3  
FTDALS4  
Fungal Lung Diseases +   
Genetic Skin Diseases +   
Greenberg Dysplasia  
Hemoptysis 
Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Cataracts  
hepatopulmonary syndrome  
hereditary angioedema +   
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
hyperimmunoglobulin syndrome +   
hyperlucent lung 
hyperphosphatemic familial tumoral calcinosis +   
hypogonadotropic hypogonadism 5 with or without anosmia +   
IMMUNODEFICIENCY 31B  
Immunodeficiency 38, with Basal Ganglia Calcification  
inherited blood coagulation disease +   
inherited metabolic disorder +   
interstitial lung disease +   
Isolated Prolactin Deficiency 
Kallmann syndrome +   
Kartagener syndrome  
Kashani Strom Utley Syndrome 
Keutel Syndrome  
Laminopathies  
Lennox-Gastaut syndrome  
Leukoencephalopathy Brain Calcifications and Cysts  
lung abscess 
Lung Agenesis +   
LUNG DAMAGE, IMMUNODEFICIENCY AND CHROMOSOME BREAKAGE SYNDROME  
Lung Injury +   
Lung Neoplasms +   
lymphangioleiomyomatosis  
maple bark strippers' lung 
Marfan syndrome +   
Matthew-Wood syndrome  
Medial Coronary Sclerosis of Infancy 
middle lobe syndrome  
MONOCARBOXYLATE TRANSPORTER 1 DEFICIENCY  
monogenic disease +   
nephrocalcinosis +   
Nephrogenic Diabetes Insipidus with Mental Retardation and Intracerebral Calcification 
Nervous System Heredodegenerative Disorders +   
newborn respiratory distress syndrome +   
Nonimmune Chronic Idiopathic Neutropenia, Adult  
normophosphatemic familial tumoral calcinosis  
obstructive lung disease +   
Ossified Ear Cartilages 
osteochondrodysplasia +   
paracoccidioidomycosis +   
Parasitic Lung Diseases +  
Parotidomegaly, Hereditary Bilateral 
phaeohyphomycosis +  
Piepkorn Karp Hickok syndrome 
platelet-type bleeding disorder 10  
pneumonia +   
pneumonic plague 
polycystic kidney disease +   
polygenic disease +   
primary hypertrophic osteoarthropathy +   
Primrose Syndrome  
progressive familial intrahepatic cholestasis +   
Pseudo-TORCH Syndrome +   
pulmonary alveolar microlithiasis  
pulmonary alveolar proteinosis +   
pulmonary artery disease +   
Pulmonary Atelectasis +   
pulmonary edema +   
pulmonary eosinophilia +   
pulmonary fibrosis +   
Pulmonary Function 
Pulmonary Hemorrhage +   
pulmonary hemosiderosis 
pulmonary hypertension +   
pulmonary immaturity 
Pulmonary Lymphangiectasia, Congenital 
pulmonary plasma cell granuloma  
pulmonary systemic sclerosis 
pulmonary tuberculosis +   
pulmonary venoocclusive disease +   
Rajab Syndrome  
Rambaud Galian Syndrome 
RASopathies  
Renal Hypophosphatemia with Intracerebral Calcifications 
respiratory failure +   
Rh deficiency syndrome  
Sacral Agenesis with Vertebral Anomalies  
Schofer Beetz Bohl Syndrome 
scimitar syndrome +   
Sclerosing Osteomalacia with Cerebral Calcification 
silo filler's disease 
sparganosis 
Spondylomegaepiphyseal Dysplasia with Upper Limb Mesomelia, Punctate Calcifications, and Deafness 
Storm Syndrome 
strongyloidiasis  
toxocariasis +   
Tropical Calcific Pancreatitis  
Vascular Calcification +   
Whyte Murphy Fallon Sly syndrome 
yellow nail syndrome +  

Synonyms
Primary IDs: MESH:C562405
Alternate IDs: OMIM:265100 ;   RDO:0012148
Xrefs: GARD:11894

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.