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Details
Link-It Detail - Human Phenotype - Abnormality of the lung
Debug Stats
  • ### Total Build Time: 48 ms 38.047 KB
  • CONCEPT_NAME gt=0 Completed: 0 ms rowSize= 198 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_DEFINITION gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
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  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 799 bytes
  • CONCEPT_CHILDREN gt=0 Completed: 0 ms rowSize= 12.951 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.112 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=48 ms Completed: 47 ms rowSize= 20.848 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.018 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the lung HP:0002088
Parents (2)
img Abnormality of the respiratory system HP:0002086
img Abnormal respiratory system morphology HP:0012252
Children (40)
img Pulmonary hypertension HP:0002092
img Pulmonary arteriovenous malformation HP:0006548
img Cystic lung disease HP:0005948
img Interstitial pulmonary disease HP:0006530
img Pneumonia HP:0002090
img Emphysema HP:0002097
img Abnormality of the pleura HP:0002103
img Pneumothorax HP:0002107
img Pulmonary fibrosis HP:0002206
img Pulmonary capillary hemangiomatosis HP:0005954
img Lung segmentation defects HP:0006525
img Bronchogenic cyst HP:0100730
img Neoplasm of the lungs HP:0100526
img Asthma HP:0002099
img Hypersensitivity pneumonitis HP:0006516
img Unilateral primary pulmonary dysgenesis HP:0006549
img Restrictive lung disease HP:0002091
img Respiratory insufficiency HP:0002093
img Congenital alveolar proteinosis HP:0006517
img Recurrent lower respiratory tract infections HP:0002783
img Dyspnea HP:0002094
img Hemoptysis HP:0002105
img Respiratory tract infection HP:0011947
img Pulmonary edema HP:0100598
img Atelectasis HP:0100750
img Pulmonary embolism HP:0002204
img Abnormal lung lobation HP:0002101
img Pulmonary infiltrates HP:0002113
img Aplasia/Hypoplasia of the lungs HP:0006703
img Diffuse reticular or finely nodular infiltrations HP:0002207
img Pulmonary venoocclusive disease HP:0006518
img Recurrent intrapulmonary hemorrhage HP:0006535
img Intraalveolar nodular calcifications HP:0006514
img Chronic lung disease HP:0006528
img Bronchopulmonary sequestration HP:0010960
img Abnormal pulmonary lymphatics HP:0006529
img Obstructive lung disease HP:0006536
img Abnormal respiratory motile cilium morphology HP:0005938
img Congenital cystic adenomatoid malformation of the lung HP:0010959
img Lung fibroma HP:0010616
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the respiratory system HP:0002086
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormal respiratory system morphology HP:0012252
Genes (742)

Species:
human : 742
Page Size
Current 25
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SpeciesGeneGeneIdGene NameEvidence
HumanPDA1100996949Patent ductus arteriosus, susceptibility to
img HP RolledUp, OMIM ID: 607411
HumanDER22T11-22100529146
HumanRCHTS100462676Roifman-Chitayat syndrome
img HP RolledUp, OMIM ID: 613328
HumanDEL17Q23.1Q23.2100415941
img HP RolledUp, OMIM ID: 613355
HumanARCODS100381211Ariculocondylar syndrome
img HP RolledUp, OMIM ID: 602483
HumanDEL19Q13.11100306978
HumanFL1100306940Follicular lymphoma, susceptibility to, 1
img HP RolledUp, OMIM ID: 613024
HumanPRBNS100301572Pierre Robin syndrome
img HP RolledUp, OMIM ID: 261800
HumanDEL2P16.1-P15100240740
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanDEL18Q100216483Chromosome 18q deletion syndrome
img HP RolledUp, OMIM ID: 601808
HumanC22DDELS100188856Chromosome 22q11.2 deletion syndrome, distal
HumanSLEB5100188798Systemic lupus erythematosus, susceptibility to, 5
img HP RolledUp, OMIM ID: 152700
HumanCFTDX100188765Myopathy, congenital, with fiber-type disproportion, X-linked
img HP RolledUp, OMIM ID: 300580
HumanAOS100188340Adams-Oliver syndrome
img HP RolledUp, OMIM ID: 100300
HumanDIP100188011interstitial pneumonitis, desquamative, familial
img HP RolledUp, OMIM ID: 263000
HumanMGS100126595Mungen syndrome
img HP RolledUp, OMIM ID: 611376
HumanAA1100034700Alopecia areata 1
HumanSNORD116-1100033413
HumanKTWS791122Klippel-Trenaunay-Weber syndrome
img HP RolledUp, OMIM ID: 149000
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
HumanHHT4791087Telangiectasia, hereditary hemorrhagic, type 4
img HP RolledUp, OMIM ID: 610655
HumanNKCD780917Natural killer cell deficiency, familial isolated
img HP RolledUp, OMIM ID: 609981
HumanSFTPA2729238surfactant protein A2
img HP RolledUp, OMIM ID: 178500
HumanMUC5B727897mucin 5B, oligomeric mucus/gel-forming
img HP RolledUp, OMIM ID: 178500
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0002088Abnormality of the lung0self