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 cerebral morphology (HP:0002060)

Parent Node:
Cerebral inclusion bodies (HP:0100314)

..Starting node
..Argyrophilic inclusion bodies (HP:0100317)

Term ID:

100317

Name:

Argyrophilic inclusion bodies

Synonym:

Agyrophilic inclusion bodies; Pick inclusion bodies

Definition:

Presence of abundant argyrophilic grains and coiled bodies on microscopic examination of brain tissue.

Comments:

Reference:

HP:0100317

Genes and Diseases:

Child Nodes:

Sister Nodes:

Cerebral hyaline bodies (HP:0100319)

Hirano bodies (HP:0100316)

Lafora bodies (HP:0100318)

Lewy bodies (HP:0100315)

Neurofibrillary tangles (HP:0002185)

Rosenthal fibers (HP:0100320)

Ubiquitin-positive cerebral inclusion bodies (HP:0012083)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100317	HP:0100317	Argyrophilic inclusion bodies	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.