Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Grandparent Node:
Cataract (HP:0000518)

Parent Node:
Age-related cataract (HP:0011141)

..Starting node
..Age-related nuclear cataract (HP:0011142)

Term ID:

11142

Name:

Age-related nuclear cataract

Synonym:

Definition:

A type of age-related cataract that primarily affects the nucleus of the lens.

Comments:

Reference:

HP:0011142

Genes and Diseases:

Child Nodes:

Sister Nodes:

Age-related cortical cataract (HP:0011143)

Age-related posterior subcapsular cataract (HP:0011144)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011142	HP:0011142	Age-related nuclear cataract	0	CL E G H

Genes (0) :

Diseases (0) :

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