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Details
Link-It Detail - Human Phenotype - Abnormality of the larynx
Debug Stats
  • ### Total Build Time: 42 ms 33.294 KB
  • CONCEPT_NAME gt=3 ms Completed: 3 ms rowSize= 200 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 197 bytes
  • Skipping details on: CONCEPT_SYNONYM gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • Skipping details on: CONCEPT_TEXT gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_SEMANTIC_TYPE gt=0 Completed: 0 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=3 ms Completed: 3 ms rowSize= 463 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 6.502 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=2 ms Completed: 2 ms rowSize= 2.121 KB
  • CONCEPT_RELATIONSHIPS gt=1 ms Completed: 1 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=27 ms Completed: 27 ms rowSize= 22.667 KB
  • CONCEPT_XREFS gt=2 ms Completed: 2 ms rowSize= 1.020 KB
  • CONCEPT_ANCILLARY gt=1 ms Completed: 1 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the larynx HP:0001600
Definition (1)
An abnormality of the `larynx` (FMA:55097).
Parents (1)
img Abnormality of the upper respiratory tract HP:0002087
Children (20)
img Laryngeal stenosis HP:0001602
img Laryngeal atresia HP:0008750
img Laryngeal edema HP:0012027
img Anteroposteriorly shortened larynx HP:0005956
img Laryngeal hypoplasia HP:0008749
img Laryngeal cyst HP:0100640
img Laryngomalacia HP:0001601
img Imperfect vocal cord adduction HP:0005934
img Laryngeal obstruction HP:0005945
img Laryngeal stridor HP:0006511
img Abnormality of the epiglottis HP:0005483
img Neoplasm of the larynx HP:0100605
img Abnormality of the aryepiglottic fold HP:0008744
img Laryngeal cleft HP:0008751
img Abnormality of the vocal cords HP:0008777
img Subglottic stenosis HP:0001607
img Abnormality of the voice HP:0001608
img Cartilaginous ossification of larynx HP:0008747
img Laryngeal calcifications HP:0008754
img Laryngeal cartilage malformation HP:0008752
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the upper respiratory tract HP:0002087
img All HP:0000001img Phenotypic abnormality HP:00001186img Abnormality of the upper respiratory tract HP:0002087
Genes (271)

Species:
human : 271
Page Size
Current 25
  Page 1 of 11
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Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanHMSN5101059903Hereditary motor and sensory neuropathy V
img HP RolledUp, OMIM ID: 600361
HumanDYT21100885773dystonia 21, torsion (autosomal dominant)
img HP RolledUp, OMIM ID: 614588
HumanDUPXQ27.3Q28100874533
img HP RolledUp, OMIM ID: 300869
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanDEL8Q13100526741Mesomelia-synostoses syndrome
img HP RolledUp, OMIM ID: 600383
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP RolledUp, OMIM ID: 606407
HumanARCODS100381211Ariculocondylar syndrome
img HP RolledUp, OMIM ID: 602483
HumanDUPXP11.23P11.22100310754
img HP RolledUp, OMIM ID: 300801
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanDUP22Q11.2100240738
img HP RolledUp, OMIM ID: 608363
HumanDYT17100216344dystonia 17
img HP RolledUp, OMIM ID: 612406
HumanDEL2Q32Q33100190983Chromosome 2q32-q33 deletion syndrome
img HP RolledUp, OMIM ID: 612313
HumanMICRODEL3Q29100188788Chromosome 3q29 microdeletion syndrome
img HP RolledUp, OMIM ID: 609425
HumanCFTDX100188765Myopathy, congenital, with fiber-type disproportion, X-linked
img HP RolledUp, OMIM ID: 300580
HumanSTUT1100049541Stuttering, familial persistent 1
img HP RolledUp, OMIM ID: 184450
HumanPTLS100038247Potocki-Lupski syndrome
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
HumanDEL17Q21.31791085
img HP RolledUp, OMIM ID: 610443
HumanSCAX3727715spinocerebellar ataxia, X-linked 3
img HP RolledUp, OMIM ID: 301790
HumanPARK12677662Parkinson disease 12 (susceptibility)
img HP RolledUp, OMIM ID: 168600
HumanSCA20407973spinocerebellar ataxia 20
img HP RolledUp, OMIM ID: 608687
HumanGDF6392255growth differentiation factor 6
img HP RolledUp, OMIM ID: 148900
HumanHSN1B378888Hereditary sensory neuropathy, type IB
img HP RolledUp, OMIM ID: 608088
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0001600Abnormality of the larynx0self