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"count": 6723,
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{
"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 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 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 44.",
"acronym": "SPGF44.",
"accession": "DI-05927",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder caused by spermatogenesis defects and characterized by the presence of acephalic spermatozoa in the semen of affected individuals. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 43.",
"acronym": "SPGF43.",
"accession": "DI-05740",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder characterized by asthenospermia due to multiple morphologic abnormalities of sperm flagella, including short, absent, coiled, and bent flagella. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 42.",
"acronym": "SPGF42.",
"accession": "DI-05739",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder characterized by almost immotile spermatozoa due to multiple morphologic abnormalities of the flagella, including short, absent, coiled, and bent flagella. Some spermatozoa also show abnormalities of the head, acrosome, midpiece, or endpiece. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 41.",
"acronym": "SPGF41.",
"accession": "DI-05694",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder characterized by oligozoospermia, severe asthenozoospermia and flagellar abnormalities such as short, absent, coiled, and irregular-caliber flagella. Some sperm show tapered heads and acrosomal abnormalities. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 40.",
"acronym": "SPGF40.",
"accession": "DI-05693",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder characterized by severely reduced or absent sperm motility, due to multiple morphologic anomalies such as absent, short, bent, coiled and irregular-caliber tails. Patient spermatozoa may also show morphologic defects of the sperm head. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 4.",
"acronym": "SPGF4.",
"accession": "DI-02748",
"synonyms": "Azoospermia due to perturbations of meiosis.; Azoospermia with maturation arrest.; Spermatogenesis arrest.; ",
"cross_references": "MeSH; D053713.",
"definition": "An infertility disorder characterized by azoospermia, a condition of having no sperm present in the ejaculate. Testicular histology shows arrest of spermatogenesis at the pachytene stage of primary spermatocytes. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 39.",
"acronym": "SPGF39.",
"accession": "DI-05668",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder characterized by asthenoteratozoospermia. Spermatozoa exhibit multiple morphologic anomalies including short, absent, irregularly shaped and coiled flagella, and abnormalities of the head and midpiece. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 38.",
"acronym": "SPGF38.",
"accession": "DI-05557",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder characterized by asthenoteratozoospermia. Spermatozoa exhibit multiple morphologic abnormalities including short, absent, coiled, bent, or irregular- caliber flagella. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 37.",
"acronym": "SPGF37.",
"accession": "DI-05556",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder characterized by asthenoteratozoospermia. Spermatozoa exhibit multiple morphologic abnormalities, primarily consisting of short or absent flagella, and neck defects at the head-tail junction. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 36.",
"acronym": "SPGF36.",
"accession": "DI-05555",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal dominant infertility disorder due to teratozoospermia, with spermatozoa showing anomalies of the head, acrosome, and nucleus. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 35.",
"acronym": "SPGF35.",
"accession": "DI-05484",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder caused by spermatogenesis defects that result in multiple abnormalities of sperm flagellum and severely impaired spermatozoa motility. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 34.",
"acronym": "SPGF34.",
"accession": "DI-05351",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder caused by spermatogenesis defects that result in multiple abnormalities of sperm flagellum, including irregular-caliber, short, coiled, or absent flagella. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 33.",
"acronym": "SPGF33.",
"accession": "DI-05350",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder caused by spermatogenesis defects that result in multiple abnormalities of sperm flagellum, including short, bent, curled, thick, or absent flagella. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 32.",
"acronym": "SPGF32.",
"accession": "DI-05325",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal dominant infertility disorder caused by spermatogenesis defects that result in non-obstructive azoospermia. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 31.",
"acronym": "SPGF31.",
"accession": "DI-05314",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder caused by spermatogenesis defects that result in oligozoospermia with a high proportion of acephalic sperm. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 30.",
"acronym": "SPGF30.",
"accession": "DI-05324",
"synonyms": null,
"cross_references": "MeSH; D007248.",
"definition": "An autosomal recessive infertility disorder caused by spermatogenesis defects that result in non-obstructive azoospermia or cryptozoospermia. ",
"keywords": null
},
{
"identifier": "Spermatogenic failure 3.",
"acronym": "SPGF3.",
"accession": "DI-03796",
"synonyms": null,
"cross_references": "MeSH; D053627.",
"definition": "A disorder characterized by primary infertility, sperm morphologic abnormalities, and moderate to severe asthenozoospermia, condition in which the percentage of progressively motile sperm is abnormally low. ",
"keywords": null
}
]
}