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Details
Link-It Detail - Human Phenotype - Abnormality of the penis
Debug Stats
  • ### Total Build Time: 27 ms 32.768 KB
  • CONCEPT_NAME gt=2 ms Completed: 2 ms rowSize= 199 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
  • 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=0 Completed: 0 ms rowSize= 459 bytes
  • CONCEPT_CHILDREN gt=3 ms Completed: 3 ms rowSize= 5.794 KB
  • CONCEPT_ANCESTRAL_ROOTS gt=0 Completed: 0 ms rowSize= 2.113 KB
  • CONCEPT_RELATIONSHIPS gt=0 Completed: 0 ms rowSize= 106 bytes
  • CONCEPT_GENES gt=22 ms Completed: 22 ms rowSize= 23.055 KB
  • CONCEPT_XREFS gt=0 Completed: 0 ms rowSize= 1.019 KB
  • CONCEPT_ANCILLARY gt=0 Completed: 0 ms rowSize= 14 bytes
  • Reload Stats
Human Phenotype (1)
Abnormality of the penis HP:0000036
Parents (1)
img Abnormality of male external genitalia HP:0000032
Children (18)
img Underdeveloped penis HP:0008632
img Diphallia HP:0100599
img Erectile abnormalities HP:0100639
img Displacement of the external urethral meatus HP:0100627
img Abnormality of corpus cavernosum HP:0100623
img Partial development of the penile shaft HP:0008708
img Micropenis HP:0000054
img Priapism HP:0200023
img Penoscrotal transposition HP:0100600
img Urethral atresia, male HP:0000052
img Chordee HP:0000041
img Neoplasia of the penis HP:0100850
img Abnormality of the preputium HP:0100587
img Hypospadias HP:0000047
img Phimosis HP:0001741
img Epispadias HP:0000039
img Enlarged penis HP:0000040
img Hypoplasia of penis HP:0008736
Ancestral Roots
RootRoot Plus OneDepthParent
img All HP:0000001img Phenotypic abnormality HP:00001188img Abnormality of male external genitalia HP:0000032
img All HP:0000001img Phenotypic abnormality HP:00001187img Abnormality of male external genitalia HP:0000032
Genes (267)

Species:
human : 267
Page Size
Current 25
  Page 1 of 11
Prior Page
Current 1
SpeciesGeneGeneIdGene NameEvidence
HumanDUP16P11.2100909384
img HP RolledUp, OMIM ID: 614671
HumanNMLFS100885786Nablus mask-like facial syndrome
img HP RolledUp, OMIM ID: 608156
HumanDEL2Q23.1100820633
img HP RolledUp, OMIM ID: 156200
HumanMLSM7100820631Myelodysplasia and leukemia syndrome with monosomy 7
img HP RolledUp, OMIM ID: 252270
HumanDEL8Q21.11100689491
img HP RolledUp, OMIM ID: 614230
HumanHYSP3100689211Hypospadias 3, autosomal
img HP RolledUp, OMIM ID: 146450
HumanDER22T11-22100529146
img HP RolledUp, OMIM ID: 609029
HumanDEL11P13100528024Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome
img HP RolledUp, OMIM ID: 194072
HumanDEL15Q24100502567Chromosome 15q24 deletion syndrome
img HP RolledUp, OMIM ID: 613406
HumanDUP17P13.3100379203
img HP RolledUp, OMIM ID: 613215
HumanDEL19Q13.11100306978
img HP RolledUp, OMIM ID: 613026
HumanDEL15Q26QTER100271921Chromosome 15q26-qter deletion syndrome
img HP RolledUp, OMIM ID: 612626
HumanDEL9P100240748Chromosome 9p deletion syndrome
img HP RolledUp, OMIM ID: 158170
HumanDEL18P100240747Chromosome 18p deletion syndrome
img HP RolledUp, OMIM ID: 146390
HumanDEL2P16.1-P15100240740
img HP RolledUp, OMIM ID: 612513
HumanDUP22Q11.2100240738
img HP RolledUp, OMIM ID: 608363
HumanDEL1P36100240737Chromosome 1p36 deletion syndrome
img HP RolledUp, OMIM ID: 607872
HumanDUP1Q21100217371Chromosome 1q21.1 duplication syndrome
img HP RolledUp, OMIM ID: 612475
HumanDEL18Q100216483Chromosome 18q deletion syndrome
img HP RolledUp, OMIM ID: 601808
HumanMICRODEL3Q29100188788Chromosome 3q29 microdeletion syndrome
img HP RolledUp, OMIM ID: 609425
HumanCFSS100188773craniofacioskeletal syndrome
img HP RolledUp, OMIM ID: 300712
HumanRNU4ATAC100151683RNA, U4atac small nuclear (U12-dependent splicing)
img HP RolledUp, OMIM ID: 210710
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
XRefs (1)

XRef Types:
hp : 1


ToppGene Datasets:
none : 1
ToppGene DatasetsXRef TypeXRef IdXRefValuesSourceTop % Rank
HPimg HP:0000036Abnormality of the penis0self