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"count": 6723,
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{
"identifier": "Spermatogenic failure 45.",
"acronym": "SPGF45.",
"accession": "DI-05965",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder caused by spermatogenesis defects resulting in severe teratozoospermia. SPGF45 is characterized by multiple morphologic abnormalities of spermatozoa flagella. Some spermatozoa also show abnormalities of the head. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 46.",
"acronym": "SPGF46.",
"accession": "DI-05966",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder caused by spermatogenesis defects resulting in asthenoteratozoospermia. SPGF46 is characterized by multiple morphologic abnormalities of sperm flagella with disorganization of axonemal and periaxonemal structures. Flagella are absent, short, coiled, angulated, and/or of irregular caliber. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 47.",
"acronym": "SPGF47.",
"accession": "DI-05967",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder caused by spermatogenesis defects resulting in asthenoteratozoospermia. SPGF47 is characterized by reduced sperm concentrations and immotile spermatozoa, with short or absent flagella as well as centriolar abnormalities. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 48.",
"acronym": "SPGF48.",
"accession": "DI-05968",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder caused by spermatogenesis defects resulting in non-obstructive azoospermia. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 49.",
"acronym": "SPGF49.",
"accession": "DI-05976",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder characterized by asthenoteratozoospermia and multiple morphologic abnormalities of the sperm flagella, primarily coiled and short flagella, with markedly reduced or absent motility. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 5.",
"acronym": "SPGF5.",
"accession": "DI-01927",
"synonyms": "Infertility associated with multi-tailed spermatozoa and excessive DNA.; Male infertility with large-headed multiflagellar polyploid spermatozoa.; ",
"cross_references": "MeSH; D007248.",
"definition": "An infertility disorder caused by spermatogenesis defects. Semen from affected men show close to 100% morphologically abnormal multiflagellar spermatozoa with low motility, oversized irregular heads, and abnormal midpiece and acrosome. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 50.",
"acronym": "SPGF50.",
"accession": "DI-05977",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder characterized by azoospermia due to meiotic arrest at the zygotene stage of prophase I. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 51.",
"acronym": "SPGF51.",
"accession": "DI-06022",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder characterized by asthenoteratozoospermia. Spermatozoa exhibit multiple morphologic abnormalities, including absent, short, bent, coiled and irregular- caliber flagella. Abnormalities of the sperm head, base, and acrosome have also been observed. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 52.",
"acronym": "SPGF52.",
"accession": "DI-06021",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder characterized by azoospermia due to meiotic arrest at the spermatocyte stage. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 53.",
"acronym": "SPGF53.",
"accession": "DI-06072",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder characterized by impaired oocyte fertilization due to oocyte activation failure, in association with structural anomalies in sperm heads. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 54.",
"acronym": "SPGF54.",
"accession": "DI-06144",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive male infertility disorder characterized by oligoteratoasthenozoospermia.Semen analysis shows markedly reduced sperm counts and severely reduced or absent sperm motility. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 55.",
"acronym": "SPGF55.",
"accession": "DI-06145",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive male infertility disorder characterized by asthenozoospermia.Semen analysis shows severely reduced sperm motility. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 56.",
"acronym": "SPGF56.",
"accession": "DI-06189",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive male infertility disorder characterized by severely reduced sperm motility, due to multiple morphologic abnormalities of the flagella. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 57.",
"acronym": "SPGF57.",
"accession": "DI-06188",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive male infertility disorder characterized by non- obstructive azoospermia, due to error-prone meiosis and spermatogenic arrest at the late pachytene stage. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 58.",
"acronym": "SPGF58.",
"accession": "DI-06203",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive male infertility disorder characterized by absent or severely reduced sperm motility, due to multiple morphological abnormalities of the sperm flagellum. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 59.",
"acronym": "SPGF59.",
"accession": "DI-06204",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive male infertility disorder characterized by non- obstructive azoospermia, due to sperm maturation arrest. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 6.",
"acronym": "SPGF6.",
"accession": "DI-01666",
"synonyms": "Acrosome malformation of spermatozoa.; Globozoospermia.; Round-headed spermatozoa.; ",
"cross_references": "MeSH; D007248.",
"definition": "An infertility disorder caused by spermatogenesis defects. The most prominent feature is the malformation of the acrosome, which can be totally absent in most severe cases. Additional features are an abnormal nuclear shape and abnormal arrangement of the mitochondria of the spermatozoon. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 60.",
"acronym": "SPGF60.",
"accession": "DI-06205",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive male infertility disorder characterized by non- obstructive azoospermia, due to sperm maturation arrest before the pachytene stage. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 61.",
"acronym": "SPGF61.",
"accession": "DI-06206",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive male infertility disorder characterized by non- obstructive azoospermia, due to complete meiotic arrest at the primary spermatocyte stage. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 62.",
"acronym": "SPGF62.",
"accession": "DI-06207",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive male infertility disorder characterized by non- obstructive azoospermia, due to complete metaphase arrest at the spermatocyte stage. ",
"keywords": null
}
]
}