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 neopterin concentration (HP:0040206)

Grandparent Node:
Abnormal CSF metabolite level (HP:0025454)

Parent Node:
Abnormal CSF neopterin level (HP:0040203)

..Starting node
..Decreased CSF neopterin level (HP:0040205)

Term ID:

40205

Name:

Decreased CSF neopterin level

Synonym:

Definition:

Decreased concentration of neopterin in the cerebrospinal fluid (CSF).

Comments:

Reference:

HP:0040205

Genes and Diseases:

Child Nodes:

Sister Nodes:

Elevated CSF neopterin level (HP:0040204)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040205	HP:0040205	Decreased CSF neopterin level	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 August 2021 release.