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:
Abnormality of the musculature of the upper arm (HP:0001457)

Grandparent Node:
Aplasia/Hypoplasia involving the musculature of the upper limbs (HP:0001467)

Parent Node:
Aplasia/Hypoplasia involving the musculature of the upper arm (HP:0001468)

..Starting node
..Aplasia/Hypoplasia of the triceps (HP:0009784)

Term ID:

9784

Name:

Aplasia/Hypoplasia of the triceps

Synonym:

Absent/small triceps; Absent/underdeveloped triceps

Definition:

Absence or underdevelopment of the triceps muscle.

Comments:

Reference:

HP:0009784

Genes and Diseases:

Child Nodes:

........

Triceps aplasia (HP:0009785)

........

Triceps hypoplasia (HP:0100855)

Sister Nodes:

Aplasia/Hypoplasia of the biceps (HP:0009782)

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	Frequency	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0009784	HP:0009784	Aplasia/Hypoplasia of the triceps	0	LMX1B CL E G H	4010	6654	OMIM:161200	Nail-Patella syndrome		165
HP:0009784	HP:0100855	Triceps hypoplasia	1	CL E G H
HP:0009784	HP:0009785	Triceps aplasia	1	LMX1B CL E G H	4010	6654	OMIM:161200	Nail-Patella syndrome	.	165

Genes (1) :LMX1B

Diseases (1) :OMIM:161200

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.