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

Parent Node:
Aplasia of the musculature (HP:0100854)

Parent Node:
Aplasia/Hypoplasia of the biceps (HP:0009782)

..Starting node
..Biceps aplasia (HP:0009783)

Term ID:

9783

Name:

Biceps aplasia

Synonym:

Absent biceps

Definition:

Absence of the biceps muscle.

Comments:

Reference:

HP:0009783

Genes and Diseases:

Child Nodes:

Sister Nodes:

Biceps hypoplasia (HP:0009007)

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:0009783	HP:0009783	Biceps aplasia	0	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.