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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
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Hemosiderosis (D006486)
Parent Node:
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Lung Diseases (D008171)
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Idiopathic pulmonary hemosiderosis (C536281)

       Child Nodes:



 Sister Nodes: 
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..expandAcute Chest Syndrome (D056586)
..expandalpha 1-Antitrypsin Deficiency (D019896) Child1
..expandalpha-2-Macroglobulin Deficiency (C566304)
..expandAnophthalmia with pulmonary hypoplasia (C537768)
..expandCystic Adenomatoid Malformation of Lung, Congenital (D015615)
..expandCystic Disease Of Lung (C563237)
..expandCystic Fibrosis (D003550) Child4
..expandHemoptysis (D006469)
..expandHepatopulmonary Syndrome (D020065)
..expandHypertension, Pulmonary (D006976) Child12
..expandIdiopathic pulmonary hemosiderosis (C536281)
..expandKashani Strom Utley syndrome (C537010)
..expandLung Abscess (D008169)
..expandLung agenesis (C537725)
..expandLung Diseases, Fungal (D008172) Child5
..expandLung Diseases, Interstitial (D017563) Child39
..expandLung Diseases, Obstructive (D008173) Child34
..expandLung Diseases, Parasitic (D008174) Child1
..expandLung Injury (D055370) Child20
..expandLung Neoplasms (D008175) Child17
..expandLung, Hyperlucent (D019568)
..expandLymphangiectasia, pulmonary, congenital (C537727)
..expandPlasma Cell Granuloma, Pulmonary (D016726)
..expandPneumonia (D011014) Child16
..expandPulmonary Alveolar Microlithiasis (C562405)
..expandPulmonary Alveolar Proteinosis (D011649) Child7
..expandPulmonary Atelectasis (D001261) Child1
..expandPulmonary Edema (D011654) Child1
..expandPulmonary Embolism (D011655) Child3
..expandPulmonary Eosinophilia (D011657) Child1
..expandPulmonary Fibrosis (D011658) Child2
..expandPULMONARY FUNCTION (OMIM:608852)
..expandPulmonary Hypoplasia, Primary (C562992)
..expandPulmonary Veno-Occlusive Disease (D011668)
..expandRapidly progressive glomerulonephritis with pulmonary hemorrhage (C538458)
..expandRespiratory Distress Syndrome, Adult (D012128)
..expandRespiratory Distress Syndrome, Newborn (D012127) Child9
..expandScimitar Syndrome (D012587) Child1
..expandSolitary Pulmonary Nodule (D003074)
..expandTetra-amelia with pulmonary hypoplasia (C536499)
..expandTuberculosis, Pulmonary (D014397) Child1
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:5706
Name:Idiopathic pulmonary hemosiderosis
Definition:
Alternative IDs:
ParentIDs:MESH:D006486|MESH:D008171
TreeNumbers:C08.381/C536281 |C18.452.565.500.500/C536281
Synonyms:Alveolar hypoventilation syndrome |Hemosiderosis, pulmonary, with deficiency of gamma-a globulin |Pulmonary hemosiderosis
Slim Mappings:Metabolic disease|Respiratory tract disease
Reference: MedGen: C536281
MeSH: C536281
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants