HTTP 200 OK
Allow: GET, POST, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept
{
"count": 6723,
"next": "https://cinder.proteo.info/api/human_diseases/?format=api&limit=20&offset=6100&ordering=synonyms",
"previous": "https://cinder.proteo.info/api/human_diseases/?format=api&limit=20&offset=6060&ordering=synonyms",
"results": [
{
"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 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 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 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": "Retinitis pigmentosa 37.",
"acronym": "RP37.",
"accession": "DI-00993",
"synonyms": null,
"cross_references": "MeSH; D012174.",
"definition": "A retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. ",
"keywords": "KW-0682:Retinitis pigmentosa.; "
},
{
"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": "Retinitis pigmentosa 36.",
"acronym": "RP36.",
"accession": "DI-02263",
"synonyms": null,
"cross_references": "MeSH; D012174.",
"definition": "A retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. ",
"keywords": "KW-0682:Retinitis pigmentosa.; "
}
]
}