Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the vasculature (HP:0002597)help
Grandparent Node:
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obsolete Abnormal globe morphology (HP:0012374)help
Parent Node:
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Abnormality of the vasculature of the eye (HP:0008047)help
..Starting node
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Red eye (HP:0025337)help
Term ID: 25337
Name: Red eye
Synonym:
Definition: A reddish appearance over the white part (sclera) of the eye ranging from a few enlarged blood vessels appearing as wiggly lines over the sclera to a bright red color completely covering to sclera.
Comments:
Reference: HP:0025337
Genes and Diseases:
 
       Child Nodes:
........expandConjunctivitis (HP:0000509) help
................... HP:0001096 Keratoconjunctivitis
................... HP:0007717 Chronic irritative conjunctivitis
................... HP:0007879 Allergic conjunctivitis
........expandSuperficial episcleral hyperemia (HP:0025339) help
........expandDeep episcleral hyperemia (HP:0025340) help
........expandConjunctival hyperemia (HP:0030953) help
................... HP:0025338 Circumlimbal hyperemia

 Sister Nodes: 
..expandAbnormal iris vasculature (HP:0007905) help
..expandAbnormal morphology of the conjunctival vasculature (HP:0008054) help
..expandAbnormal retinal vascular morphology (HP:0008046) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025337HP:0025337Red eye0 CL E G H
HP:0025337HP:0025337Red eye1 CL E G H
HP:0025337HP:0025337Red eye2 CL E G H
HP:0025337HP:0025337Red eye3 CL E G H


Genes (83) :AIRE B2M BLNK BTD BTK BTNL2 C4A CCR1 CD19 CD79A CD79B COL7A1 CR2 DDB2 DKC1 DNASE1L3 ERAP1 ERCC2 ERCC6 ERF FAS FERMT1 FGFR2 FOXC2 FOXE3 GATA1 GJB2 GJB6 GNAS HLA-B HLA-DRB1 HLCS ICOS IGHM IGLL1 IGSF3 IKZF1 IL10 IL12A IL12A-AS1 IL23R KLRC4 LBR LMNA LRBA LRRC8A MBTPS2 MEFV MPLKIP NLRC4 NLRP1 NLRP3 PIK3R1 PITX3 PLG POLH PSMB4 PSMB8 PSMB9 RAG1 RAG2 RNF125 SAMD9 SCN9A SLC39A4 STAT4 STX16 TCF3 TFRC TLR4 TNFRSF13B TNFRSF13C TNFRSF1A TNXB TP63 UBAC2 UROS USB1 WAS WIPF1 XPA XPC ZMPSTE24

Diseases (71) :33110 253260 47 300755 307200 240500 613493 612692 226600 278740 305000 36412 278730 278800 207 2908 123500 33001 153400 129500 94089 79443 79444 36426 607594 601495 149700 614700 2273 308800 47045 575 191900 120100 148200 217090 278750 617591 256040 601457 610455 37 616740 32960 142680 103285 106260 263700 604173 906 278700 278720 240300 79241 79277 79242 97231 69085 314652 797 117 601675 88632 148210 779 740 234050 617388 616260 133020 285
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.