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Details
Link-It Detail - Human Phenotype - Abnormality of genital physiology
Debug Stats
  • ### Total Build Time: 41 ms 26.320 KB
  • CONCEPT_NAME gt=4 ms Completed: 4 ms rowSize= 208 bytes
  • CONCEPT_SOLR_HIT_STATS gt=0 Completed: 0 ms rowSize= 14 bytes
  • CONCEPT_DEFINITION gt=0 Completed: 0 ms rowSize= 249 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=1 ms Completed: 1 ms rowSize= 14 bytes
  • Skipping details on: CONCEPT_NAMESPACE gt=NONE 0 Completed: 0 ms rowSize= 0 bytes
  • CONCEPT_PARENTS gt=0 Completed: 0 ms rowSize= 454 bytes
  • CONCEPT_CHILDREN gt=4 ms Completed: 4 ms rowSize= 1.389 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 1.169 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=27 ms Completed: 27 ms rowSize= 21.701 KB
  • CONCEPT_XREFS gt=5 ms Completed: 5 ms rowSize= 1.027 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of genital physiology HP:0000080
Definition (1)
An `abnormal` (PATO:0000460) `functionality` (PATO:0001509) of the `genital system` (FMA:7160).
Parents (1)
img Abnormality of the genital system HP:0000078
Children (4)
img Decreased fertility HP:0000144
img Functional abnormality of male internal genitalia HP:0000025
img Impotence HP:0000802
img Hypogonadism HP:0000135
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001185img Abnormality of the genital system HP:0000078
Genes (208)

Species:
human : 208
Page Size
Current 25
  Page 1 of 9
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDUPXQ27.3Q28100874533
img HP RolledUp, OMIM ID: 300869
HumanSPG46100861438spastic paraplegia 46 (autosomal recessive)
img HP RolledUp, OMIM ID: 614409
HumanSPGFX2100820759Spermatogenic failure, X-linked, 2
HumanDFNB81100653390deafness, autosomal recessive 81
img HP RolledUp, OMIM ID: 614129
HumanMYMY4100653379Moyamoya disease 4
img HP RolledUp, OMIM ID: 300845
HumanSRXX210065337846XX sex reversal 2
img HP RolledUp, OMIM ID: 278850
HumanDEL2P21100415942Hypotonia-cystinuria syndrome
img HP RolledUp, OMIM ID: 606407
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanDEL15Q15.3100240731
img HP RolledUp, OMIM ID: 611102
HumanENDO1100188863Endometriosis, susceptibility to, 1
img HP RolledUp, OMIM ID: 131200
HumanDFCTRPS100188774Deafness, cataract, retinitis pigmentosa, and sperm abnormalities
HumanSNORD116-1100033413
img HP RolledUp, OMIM ID: 176270
HumanPWRN1791114Prader-Willi region non-protein coding RNA 1
img HP RolledUp, OMIM ID: 176270
HumanGTF2H5404672general transcription factor IIH, polypeptide 5
img HP RolledUp, OMIM ID: 601675
HumanHSN1B378888Hereditary sensory neuropathy, type IB
img HP RolledUp, OMIM ID: 608088
HumanDNAAF3352909dynein, axonemal, assembly factor 3
HumanCCDC39339829coiled-coil domain containing 39
img HP RolledUp, OMIM ID: 613807
HumanSNORD115-1338433
img HP RolledUp, OMIM ID: 176270
HumanKLHL10317719kelch-like family member 10
img HP RolledUp, OMIM ID: 615081
HumanDPY19L2283417dpy-19-like 2 (C. elegans)
img HP RolledUp, OMIM ID: 613958
HumanRSPH9221421radial spoke head 9 homolog (Chlamydomonas)
img HP RolledUp, OMIM ID: 612650
HumanBBS12166379Bardet-Biedl syndrome 12
img HP RolledUp, OMIM ID: 209900
HumanSTRC161497stereocilin
img HP RolledUp, OMIM ID: 612997
HumanHFE2148738hemochromatosis type 2 (juvenile)
img HP RolledUp, OMIM ID: 602390
HumanPWAR1145624Prader Willi/Angelman region RNA 1
img HP RolledUp, OMIM ID: 176270
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000080Abnormality of genital physiology0self