WormMine

WS297

Intermine data mining platform for C. elegans and related nematodes

Disease Ontology : DOID:0070188 spermatogenic failure 1 Disease Ontology

Namespace  disease_ontology Obsolete  false
Description  A spermatogenic failure that is characterized by autosomal recessive inheritance of spermatogenic failure resulting from meiotic defects.

1 Ontology

Name
Disease Ontology

7 Parents

Identifier Name Description
DOID:7 disease of anatomical entity A disease that manifests in a defined anatomical structure.
DOID:4 disease A disease is a disposition (i) to undergo pathological processes that (ii) exists in an organism because of one or more disorders in that organism.
DOID:48 male reproductive system disease A reproductive system disease that affects male reproductive organs.
DOID:15 reproductive system disease A disease of anatomical entity that is located_in reproductive system organs.
DOID:12336 male infertility  
DOID:0111910 spermatogenic failure A male infertility characterized by disruption of the process of sperm development from diploid cells into mature haploid spermatozoa.
DOID:0070188 spermatogenic failure 1 A spermatogenic failure that is characterized by autosomal recessive inheritance of spermatogenic failure resulting from meiotic defects.

6 Relations

Relationship
Parent Term . Identifier

Child Term . Identifier
is_a DOID:0111910 DOID:0070188
is_a DOID:4 DOID:0070188
is_a DOID:7 DOID:0070188
is_a DOID:12336 DOID:0070188
is_a DOID:48 DOID:0070188
is_a DOID:15 DOID:0070188

3 Synonyms

Name Type
oligochiasmatic infertility synonym
oligosynaptic infertility synonym
SPGF1 synonym