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:
Behavioral abnormality (HP:0000708)

Parent Node:
Autistic behavior (HP:0000729)

..Starting node
..Alexithymia (HP:0031433)

Term ID:

31433

Name:

Alexithymia

Synonym:

Unaware of others' emotions

Definition:

A deficit in emotional awareness characterized by difficulties in recognizing and expressing feelings and emotions manifested as a limited ability to respond to facial clues or other signs of emotions in others often accompanied by detached connections to others.

Comments:

Reference:

HP:0031433

Genes and Diseases:

Child Nodes:

Sister Nodes:

Autism (HP:0000717)

Autism with high cognitive abilities (HP:0000753)

Impaired social interactions (HP:0000735)

Restrictive behavior (HP:0000723)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031433	HP:0031433	Alexithymia	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.

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