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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 3  
age related macular degeneration 8  
Alagille syndrome  
alpha 1-antitrypsin deficiency  
Alpha-2-Deficient Collagen Disease 
Alpha-2-Macroglobulin Deficiency 
alveolar echinococcosis  
Aortic Valve, Calcification of  
apparent mineralocorticoid excess syndrome  
Aquaporin 1 Deficiency 
ataxic cerebral palsy 
atrial heart septal defect 3  
atrial heart septal defect 4  
autoimmune lymphoproliferative syndrome +   
Bacterial Lung Diseases +   
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  
Calcific Aortic Disease with Immunologic Abnormalities, Familial 
cataract 23  
cataract 25 
cataract 26 multiple types 
cataract 27  
cataract 28 
Cenani-Lenz syndactyly syndrome  
Cerebroretinal Microangiopathy with Calcifications and Cysts +   
CHARGE syndrome  
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 +   
CREST syndrome  
Cystic Adenomatoid Malformation of Lung, Congenital 
Cystic Disease of Lung 
cystic echinococcosis  
cystic fibrosis +   
desquamative interstitial pneumonia  
diffuse idiopathic skeletal hyperostosis +   
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 
frontotemporal dementia and/or amyotrophic lateral sclerosis-3  
frontotemporal dementia and/or amyotrophic lateral sclerosis-4  
Fungal Lung Diseases +   
Genetic Skin Diseases +   
Greenberg dysplasia  
Hemorrhagic Destruction of the Brain, Subependymal Calcification, and Cataracts  
hepatopulmonary syndrome  
hereditary angioedema +   
hereditary arterial and articular multiple calcification syndrome +   
Hereditary Bilateral Parotidomegaly 
Hereditary Epistaxis 
Hereditary Eye Diseases +   
hereditary lymphedema +   
Hereditary Neoplastic Syndromes +   
hyperlucent lung 
hyperphosphatemic familial tumoral calcinosis +   
hypogonadotropic hypogonadism 5 with or without anosmia +   
inherited metabolic disorder +   
interstitial lung disease +   
Isolated Prolactin Deficiency 
Kallmann syndrome +   
Kashani Strom Utley Syndrome 
Keutel Syndrome  
Labrune Syndrome  
Lennox-Gastaut syndrome  
lung abscess 
Lung Agenesis +   
Lung Damage, Immunodeficiency and Chromosome Breakage Syndrome  
Lung Injury +   
Lung Neoplasms +   
maple bark strippers' lung 
Marfan syndrome +   
Medial Coronary Sclerosis of Infancy  
middle lobe syndrome  
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 +  
phaeohyphomycosis +  
Piepkorn Karp Hickok syndrome 
pneumonia +   
pneumonic plague 
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 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 Interstitial Lung Disease with Brain Calcifications +   
Rambaud Galian Syndrome 
Renal Hypophosphatemia with Intracerebral Calcifications 
respiratory failure +   
Sacral Agenesis with Vertebral Anomalies  
Schofer Beetz Bohl Syndrome 
scimitar syndrome +   
Sclerosing Osteomalacia with Cerebral Calcification 
silo filler's disease 
Spondylomegaepiphyseal Dysplasia with Upper Limb Mesomelia, Punctate Calcifications, and Deafness 
Storm Syndrome 
syndromic microphthalmia 9  
toxocariasis +   
Tropical Calcific Pancreatitis  
Vascular Calcification +   
Whyte Murphy Fallon Sly syndrome 
yellow nail syndrome +  

Primary IDs: MESH:C562405
Alternate IDs: OMIM:265100 ;   RDO:0012148
Xrefs: GARD:11894 ;   ICD10CM:J84.02 ;   ICD9CM:516.2

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