Human Phenotype Ontology 
Grandparent Node:
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Abnormal anterior eye segment morphology (HP:0004328)help
Parent Node:
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Abnormal anterior chamber morphology (HP:0000593)help
..Starting node
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Shallow anterior chamber (HP:0000594)help
Term ID: 594
Name: Shallow anterior chamber
Synonym:
Definition: Reduced depth of the anterior chamber, i.e., the anteroposterior distance between the cornea and the iris is decreased.
Comments:
Reference: HP:0000594
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal trabecular meshwork morphology (HP:0012630) help
..expandAbsent anterior chamber of the eye (HP:0008037) help
..expandAnterior chamber cells (HP:0025560) help
..expandAnterior chamber cyst (HP:0025311) help
..expandAnterior chamber flare (HP:0031616) help
..expandAnterior chamber inflammatory cells (HP:0031701) help
..expandAnterior chamber red blood cells (HP:0031702) help
..expandAnterior chamber synechiae (HP:0007833) help
..expandCorneolenticular adhesion (HP:0011485) help
..expandDeep anterior chamber (HP:0007765) help
..expandHypopyon (HP:0031615) help
..expandOcular anterior segment dysgenesis (HP:0007700) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0000594HP:0000594Shallow anterior chamber0ADAMTS10 CL E G H81794277600Weill-Marchesani syndrome 1277600C1869114OMIM11516513201608990
HP:0000594HP:0000594Shallow anterior chamber0ATOH7 CL E G H220202221900Persistent hyperplastic primary vitreous, autosomal recessive221900C1857299OMIM194113907609875
HP:0000594HP:0000594Shallow anterior chamber0FBN1 CL E G H2200608328Weill-Marchesani syndrome 2608328C1869115OMIM1272142843603134797
HP:0000594HP:0000594Shallow anterior chamber0LTBP2 CL E G H4053614819Weill-Marchesani syndrome 3614819C3553785OMIM1292996715602091
HP:0000594HP:0000594Shallow anterior chamber0NDP CL E G H4693310600Atrophia bulborum hereditaria310600C0266526OMIM11672077678300658
HP:0000594HP:0000594Shallow anterior chamber0RAB18 CL E G H22931614222Warburg micro syndrome 3614222C3280203OMIM1515414244602207
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0000594HP:0000594Shallow anterior chamber0TSPAN12 CL E G H23554613310Exudative vitreoretinopathy 5613310C2750079OMIM05110321641613138


Genes (7) :ADAMTS10 ATOH7 FBN1 LTBP2 NDP RAB18 TSPAN12

Diseases (7) :277600 221900 608328 614819 310600 614222 613310
 

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