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 autonomic nervous system morphology (HP:0012331)

Grandparent Node:
Abnormal intestine morphology (HP:0002242)

Parent Node:
Abnormality of enteric nervous system morphology (HP:0025028)

..Starting node
..Abnormality of enteric neuron morphology (HP:0025029)

Term ID:

25029

Name:

Abnormality of enteric neuron morphology

Synonym:

Definition:

Comments:

Reference:

HP:0025029

Genes and Diseases:

Child Nodes:

........

Enteric neuronal degeneration (HP:0025030)

........

Enteric intraneuronal nuclear inclusion bodies (HP:0030938)

Sister Nodes:

Abnormality of enteric ganglion morphology (HP:0004362)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025029	HP:0025029	Abnormality of enteric neuron morphology	0	CL E G H
HP:0025029	HP:0025030	Enteric neuronal degeneration	1	CL E G H
HP:0025029	HP:0030938	Enteric intraneuronal nuclear inclusion bodies	1	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.