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:
Abnormality of urine homeostasis (HP:0003110)

Parent Node:
Abnormal urinary color (HP:0012086)

..Starting node
..Dark yellow urine (HP:0040321)

Term ID:

40321

Name:

Dark yellow urine

Synonym:

Definition:

An abnormal dark-yellow color of the urine.

Comments:

Reference:

HP:0040321

Genes and Diseases:

Child Nodes:

Sister Nodes:

Blue urine (HP:0040317)

Dark urine (HP:0040319)

Purple urine (HP:0040322)

Red urine (HP:0040318)

Red-brown urine (HP:0040320)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040321	HP:0040321	Dark yellow urine	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.