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Details
Link-It Detail - Human Phenotype - Abnormal respiratory system morphology
Debug Stats
  • ### Total Build Time: 252 ms 19.181 KB
  • CONCEPT_NAME gt=11 ms Completed: 11 ms rowSize= 213 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 200 bytes
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  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 458 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 1.760 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.173 KB
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  • CONCEPT_GENES gt=235 ms Completed: 235 ms rowSize= 14.221 KB
  • CONCEPT_XREFS gt=1 ms Completed: 1 ms rowSize= 1.032 KB
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  • Reload Stats
Human Phenotype (1)
Abnormal respiratory system morphology HP:0012252
Definition (1)
A structural anomaly of the respiratoy system.
Parents (1)
img Abnormality of the respiratory system HP:0002086
Children (5)
img Abnormal respiratory epithelium morphology HP:0012253
img Abnormality of the diaphragm HP:0000775
img Abnormality of the upper respiratory tract HP:0002087
img Abnormality of pulmonary situs HP:0011615
img Abnormality of the lung HP:0002088
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001184img Abnormality of the respiratory system HP:0002086
Genes (922)

Species:
human : 922
Page Size
Current 25
  Page 1 of 37
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanHMSN5101059903Hereditary motor and sensory neuropathy V
HumanPDA1100996949Patent ductus arteriosus, susceptibility to
HumanDYT21100885773dystonia 21, torsion (autosomal dominant)
HumanDUP17Q12100884129Chromosome 17q12 duplication syndrome
HumanDUPXQ27.3Q28100874533
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanDEL1Q41Q42100529242Chromosome 1q41-q42 deletion syndrome
HumanDER22T11-22100529146
HumanDEL8Q13100526741Mesomelia-synostoses syndrome
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
HumanRCHTS100462676Roifman-Chitayat syndrome
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
HumanDEL17Q23.1Q23.2100415941
HumanARCODS100381211Ariculocondylar syndrome
HumanDUPXP11.23P11.22100310754
HumanDEL19Q13.11100306978
HumanFL1100306940Follicular lymphoma, susceptibility to, 1
HumanPRBNS100301572Pierre Robin syndrome
HumanDEL9P100240748Chromosome 9p deletion syndrome
HumanDEL2P16.1-P15100240740
HumanDUP22Q11.2100240738
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
HumanDEL18Q100216483Chromosome 18q deletion syndrome
HumanDYT17100216344dystonia 17
HumanDEL2Q32Q33100190983Chromosome 2q32-q33 deletion syndrome
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0012252Abnormal respiratory system morphology0self