Online Mendelian Inheritance in Man

Last uploaded: January 31, 2024
Preferred Name

SPERMATOGENIC FAILURE, Y-LINKED, 1

Synonyms

INCOMPLETE SERTOLI CELL-ONLY SYNDROME

SERTOLI CELL-ONLY SYNDROME, Y-LINKED

HYPOSPERMATOGENESIS

SERTOLI CELL-ONLY SYNDROME, TYPE II

SPGFY1

SERTOLI CELL-ONLY SYNDROME, TYPE I

ID

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

altLabel

INCOMPLETE SERTOLI CELL-ONLY SYNDROME

SERTOLI CELL-ONLY SYNDROME, Y-LINKED

HYPOSPERMATOGENESIS

SERTOLI CELL-ONLY SYNDROME, TYPE II

SPGFY1

SERTOLI CELL-ONLY SYNDROME, TYPE I

cui

C1839074

C4551960

C1839075

C4048572

C1839073

Gene Locus

Yq11

Gene Symbol

SPGFY1

CYDELq11

DELYq11

Has manifestation

http://purl.bioontology.org/ontology/OMIM/MTHU062248

http://purl.bioontology.org/ontology/OMIM/MTHU072484

http://purl.bioontology.org/ontology/OMIM/MTHU072483

http://purl.bioontology.org/ontology/OMIM/MTHU037275

MIMTYPEMEANING

Phenotype description, molecular basis known.

notation

400042

OMIM Entry Type

3

OMIM MimType Value

pound

prefLabel

SPERMATOGENIC FAILURE, Y-LINKED, 1

Scope Statement

Caused by mutation in the ubiquitin-specific protease-9, Y chromosome gene (USP9Y, 400005) [MOLECULAR BASIS]

tui

T047

T033

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