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About:
spermatogenic failure 20
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An Entity of Type :
owl:Class
, within Data Space :
linkeddata.uriburner.com:28898
associated with source
document(s)
New Facet based on Instances of this Class
Attributes
Values
type
Class
subClassOf
autosomal recessive disease
spermatogenic failure
nodeID://b50939832
label
spermatogenic failure 20
described by
https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id
DOID:0070166
database_cross_reference
OMIM:617593
has_exact_synonym
SPGF20
(en)
has_obo_namespace
disease_ontology
http://purl.obolib...g/obo/IAO_0000115
A male infertility characterized by autosomal recessive inheritance of sperm flagellar morphological abnormalities that has_material_basis_in mutation in the CFAP44 gene on chromosome 3q13.
is
topic
of
Human Disease Ontology
is
annotatedSource
of
nodeID://b50939833
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