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:
Abnormal circulating nucleobase concentration (HP:0010932)

Parent Node:
Abnormal circulating monocarboxylic acid concentration (HP:0010996)

Parent Node:
Abnormal circulating pyrimidine concentration (HP:0004353)

..Starting node
..obsolete Increased urinary orotic acid concentration (HP:0010928)

Term ID:

10928

Name:

obsolete Increased urinary orotic acid concentration

Synonym:

Definition:

Comments:

Reference:

HP:0010928

Genes and Diseases:

Child Nodes:

........

Oroticaciduria (HP:0003218)

........

Orotic acid crystalluria (HP:0003526)

Sister Nodes:

Deficient excision of UV-induced pyrimidine dimers in DNA (HP:0003213)

Reduced dihydropyrimidine dehydrogenase level (HP:0003654)

Reduced orotidine 5-prime phosphate decarboxylase level (HP:0003267)

Uraciluria (HP:0012127)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010928	HP:0010928	obsolete Increased urinary orotic acid concentration	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.