Online Mendelian Inheritance in Man

Last uploaded: January 29, 2019
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Preferred Name

SPERMATOGENIC FAILURE, Y-LINKED, 1
Synonyms

SERTOLI CELL-ONLY SYNDROME, TYPE I
ID

http://purl.bioontology.org/ontology/OMIM/400042
altLabel

SERTOLI CELL-ONLY SYNDROME, TYPE I

SERTOLI CELL-ONLY SYNDROME, TYPE II

HYPOSPERMATOGENESIS

SERTOLI CELL-ONLY SYNDROME, Y-LINKED

SPGFY1

INCOMPLETE SERTOLI CELL-ONLY SYNDROME
cui

C1839073

C1839075

C0028960

C1839074
Gene Locus

Yq11
Gene Symbol

SPGFY1

CYDELq11

DELYq11
MIMTYPEMEANING

Phenotype description, molecular basis known.
notation

400042
OMIM Entry Type

3
OMIM MimType Value

pound
prefLabel

SPERMATOGENIC FAILURE, Y-LINKED, 1
tui

T047
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http://purl.bioontology.org/ontology/MESH/D009845 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MESH/C537587 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/ICD10CM/N46.11 International Classification of Diseases, Version 10 - Clinical Modification CUI
http://purl.bioontology.org/ontology/MESH/C564032 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/MEDLINEPLUS/C0028960 MedlinePlus Health Topics CUI
http://purl.bioontology.org/ontology/MESH/C564033 Medical Subject Headings CUI
http://purl.bioontology.org/ontology/ICD10CM/N46.1 International Classification of Diseases, Version 10 - Clinical Modification CUI