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:
Hyperpigmentation of the fundus (HP:0011512)

Parent Node:
Congenital hypertrophy of retinal pigment epithelium (HP:0007649)

..Starting node
..Solitary congenital hypertrophy of retinal pigment epithelium (HP:0011528)

Term ID:

11528

Name:

Solitary congenital hypertrophy of retinal pigment epithelium

Synonym:

Single isolated CHRPE; Single isolated congenital hypertrophy of retinal pigment epithelium

Definition:

Sharply demarcated hyperpigmentation which is congenital found in around 3-5% of the population and of no functional significance.

Comments:

Reference:

HP:0011528

Genes and Diseases:

Child Nodes:

Sister Nodes:

Grouped congenital hypertrophy of retinal pigment epithelium (HP:0030504)

Multiple bilateral congenital hypertrophy of retinal pigment epithelium (HP:0011529)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011528	HP:0011528	Solitary congenital hypertrophy of retinal pigment epithelium	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.