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:
Avascular necrosis (HP:0010885)

Parent Node:
Abnormality of the os naviculare pedis (HP:0100339)

Parent Node:
Juvenile aseptic necrosis (HP:0100323)

..Starting node
..Morbus Koehler (HP:0010888)

Term ID:

10888

Name:

Morbus Koehler

Synonym:

Definition:

Morbus Koehler is a Juvenile aseptic necrosis affecting the Os naviculare pedis.

Comments:

Reference:

HP:0010888

Genes and Diseases:

Child Nodes:

Sister Nodes:

Avascular necrosis of the capital femoral epiphysis (HP:0005743)

Morbus Kienboeck (HP:0010889)

Morbus Osgood-Schlatter (HP:0010890)

Morbus Scheuermann (HP:0010891)

Osteochondrosis (HP:0040188)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010888	HP:0010888	Morbus Koehler	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.