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:
Neoplasm of the anterior pituitary (HP:0011750)

Parent Node:
Pituitary adenoma (HP:0002893)

..Starting node
..Pituitary acidophilic stem cell adenoma (HP:0011758)

Term ID:

11758

Name:

Pituitary acidophilic stem cell adenoma

Synonym:

Definition:

Comments:

Reference:

HP:0011758

Genes and Diseases:

Child Nodes:

Sister Nodes:

Pituitary corticotropic cell adenoma (HP:0008291)

Pituitary gonadotropic cell adenoma (HP:0011759)

Pituitary growth hormone cell adenoma (HP:0011760)

Pituitary null cell adenoma (HP:0011761)

Pituitary prolactin cell adenoma (HP:0006767)

Pituitary thyrotropic cell adenoma (HP:0011762)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011758	HP:0011758	Pituitary acidophilic stem cell adenoma	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.