Hearing Loss Disease Portal


 
Switch to table view
Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expand
Lung Diseases (D008171)
..Starting node
..expand
Lung agenesis (C537725)

       Child Nodes:



 Sister Nodes: 
..expand46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS (OMIM:611812)
..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:6560
Name:Lung agenesis
Definition:
Alternative IDs:
ParentIDs:MESH:D008171
TreeNumbers:C08.381/C537725
Synonyms:Congenital lung agenesis |Pulmonary agenesis |Unilateral lobar pulmonary agenesis |Unilateral lung agenesis
Slim Mappings:Respiratory tract disease
Reference: MedGen: C537725
MeSH: C537725
OMIM: 601612;

Genes:
Phenotypes
1 HP:0000007Autosomal recessive inheritance
2 HP:0003577Congenital onset
3 HP:0001671Abnormal cardiac septum morphology
4 HP:0005944Bilateral lung agenesis
5 HP:0001680Coarctation of aorta
6 HP:0003811Neonatal death
7 HP:0001643Patent ductus arteriosus
8 HP:0002093Respiratory insufficiency
9 HP:0100682Tracheal atresia
Disease Causing ClinVar Variants