Human Phenotype Ontology 
Grandparent Node:
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Abnormal anterior chamber morphology (HP:0000593)help
Parent Node:
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Anterior chamber synechiae (HP:0007833)help
..Starting node
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Posterior synechiae of the anterior chamber (HP:0011484)help
Term ID: 11484
Name: Posterior synechiae of the anterior chamber
Synonym: Iridolenticular adhesions; Posterior synechiae
Definition: Adhesions between the iris and the lens.
Comments:
Reference: HP:0011484
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAnterior synechiae of the anterior chamber (HP:0011483) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011484HP:0011484Posterior synechiae of the anterior chamber0ATOH7 CL E G H22020213907OMIM:221900Persistent hyperplastic primary vitreous, autosomal recessive.4
HP:0011484HP:0011484Posterior synechiae of the anterior chamber0CYP1B1 CL E G H15452597OMIM:617315ANTERIOR SEGMENT DYSGENESIS 6; ASGD6101
HP:0011484HP:0011484Posterior synechiae of the anterior chamber0FOXC1 CL E G H22963800OMIM:602482Axenfeld-rieger syndrome, type 363
HP:0011484HP:0011484Posterior synechiae of the anterior chamber0FOXE3 CL E G H23013808OMIM:610256Anterior segment dysgenesis 2.23
HP:0011484HP:0011484Posterior synechiae of the anterior chamber0HMX1 CL E G H31665017OMIM:612109Oculoauricular syndrome2
HP:0011484HP:0011484Posterior synechiae of the anterior chamber0LCA5 CL E G H16769131923ORPHA:364055Severe early-childhood-onset retinal dystrophyHP:0040283 - Occasional70
HP:0011484HP:0011484Posterior synechiae of the anterior chamber0LRAT CL E G H92276685ORPHA:364055Severe early-childhood-onset retinal dystrophyHP:0040283 - Occasional62
HP:0011484HP:0011484Posterior synechiae of the anterior chamber0MIR204 CL E G H40698731582OMIM:616722Retinal dystrophy and iris coloboma with or without congenital cataract.1
HP:0011484HP:0011484Posterior synechiae of the anterior chamber0RPE65 CL E G H612110294ORPHA:364055Severe early-childhood-onset retinal dystrophyHP:0040283 - Occasional129
HP:0011484HP:0011484Posterior synechiae of the anterior chamber0SPATA7 CL E G H5581220423ORPHA:364055Severe early-childhood-onset retinal dystrophyHP:0040283 - Occasional48


Genes (10) :ATOH7 CYP1B1 FOXC1 FOXE3 HMX1 LCA5 LRAT MIR204 RPE65 SPATA7

Diseases (7) :OMIM:221900 OMIM:617315 OMIM:602482 OMIM:610256 OMIM:612109 ORPHA:364055 OMIM:616722
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.