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:
Abnormal sweat gland morphology (HP:0000971)

Parent Node:
Aplasia/Hypoplasia of the sweat glands (HP:0011135)

..Starting node
..Axillary apocrine gland hypoplasia (HP:0007397)

Term ID:

7397

Name:

Axillary apocrine gland hypoplasia

Synonym:

Definition:

Developmental hypoplasia of the apocrine sweat glands in the region of the axilla.

Comments:

Reference:

HP:0007397

Genes and Diseases:

Child Nodes:

Sister Nodes:

Aplasia of the sweat glands (HP:0011136)

Aplasia/Hypoplastia of the eccrine sweat glands (HP:0007592)

Hypoplastic sweat glands (HP:0007387)

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:0007397	HP:0007397	Axillary apocrine gland hypoplasia	0	TBX3 CL E G H	6926	11602	OMIM:181450	Ulnar-Mammary syndrome	.	100

Genes (1) :TBX3

Diseases (1) :OMIM:181450

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