Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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:
Anemia of inadequate production (HP:0010972)

Parent Node:
Macrocytic anemia (HP:0001972)

..Starting node
..Hyperchromic macrocytic anemia (HP:0004857)

Term ID:

4857

Name:

Hyperchromic macrocytic anemia

Synonym:

Hyperchromic macrocytic anaemia

Definition:

A type of anemia characterized by abnormally large erythrocytes with abnormally high amounts of haemoglobin.

Comments:

Reference:

HP:0004857

Genes and Diseases:

Child Nodes:

Sister Nodes:

Macrocytic dyserythropoietic anemia (HP:0005532)

Megaloblastic anemia (HP:0001889)

Refractory macrocytic anemia (HP:0004861)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0004857	HP:0004857	Hyperchromic macrocytic anemia	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.