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 hard palate morphology (HP:0100737)

Grandparent Node:
Oral cleft (HP:0000202)

Parent Node:
Cleft palate (HP:0000175)

..Starting node
..obsolete Cleft secondary palate (HP:0410004)

Term ID:

410004

Name:

obsolete Cleft secondary palate

Synonym:

Definition:

Comments:

Reference:

HP:0410004

Genes and Diseases:

Child Nodes:

........

Cleft soft palate (HP:0000185)

................... HP:0011819 Submucous cleft soft palate
................... HP:0410032 Cleft of uvula

........

Cleft hard palate (HP:0410005)

................... HP:0010289 Cleft of alveolar ridge of maxilla

Sister Nodes:

Cleft maxillary alveolus (HP:0410003)

Median cleft palate (HP:0009099)

Non-midline cleft palate (HP:0100338)

Submucous cleft of soft and hard palate (HP:0410031)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0410004	HP:0410004	obsolete Cleft secondary palate	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.