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=2980&ordering=synonyms",
"previous": "https://cinder.proteo.info/api/human_diseases/?format=api&limit=20&offset=2940&ordering=synonyms",
"results": [
{
"identifier": "Non-syndromic orofacial cleft 10.",
"acronym": "OFC10.",
"accession": "DI-02972",
"synonyms": "Non-syndromic cleft lip/palate 10.; Non-syndromic cleft lip with or without cleft palate 10.; Orofacial cleft 10.; ",
"cross_references": "MeSH; D002971.",
"definition": "A birth defect consisting of cleft lips with or without cleft palate. Cleft lips are associated with cleft palate in two-third of cases. A cleft lip can occur on one or both sides and range in severity from a simple notch in the upper lip to a complete opening in the lip extending into the floor of the nostril and involving the upper gum. ",
"keywords": null
},
{
"identifier": "Non-syndromic orofacial cleft 5.",
"acronym": "OFC5.",
"accession": "DI-00826",
"synonyms": "Non-syndromic cleft lip/palate 5.; Non-syndromic cleft lip with or without cleft palate 5.; Orofacial cleft 5.; ",
"cross_references": "MeSH; D002971.",
"definition": "A birth defect consisting of cleft lips with or without cleft palate. Cleft lips are associated with cleft palate in two-third of cases. A cleft lip can occur on one or both sides and range in severity from a simple notch in the upper lip to a complete opening in the lip extending into the floor of the nostril and involving the upper gum. ",
"keywords": null
},
{
"identifier": "Non-syndromic orofacial cleft 6.",
"acronym": "OFC6.",
"accession": "DI-00827",
"synonyms": "Non-syndromic cleft lip/palate 6.; Non-syndromic cleft lip with or without cleft palate 6.; Orofacial cleft 6.; ",
"cross_references": "MeSH; D002971.",
"definition": "A birth defect consisting of cleft lips with or without cleft palate. Cleft lips are associated with cleft palate in two-third of cases. A cleft lip can occur on one or both sides and range in severity from a simple notch in the upper lip to a complete opening in the lip extending into the floor of the nostril and involving the upper gum. ",
"keywords": null
},
{
"identifier": "Non-syndromic orofacial cleft 7.",
"acronym": "OFC7.",
"accession": "DI-00828",
"synonyms": "Non-syndromic cleft lip/palate 7.; Non-syndromic cleft lip with or without cleft palate 7.; Orofacial cleft 7.; ",
"cross_references": "MeSH; D002971.",
"definition": "A birth defect consisting of cleft lips with or without cleft palate. Cleft lips are associated with cleft palate in two-third of cases. A cleft lip can occur on one or both sides and range in severity from a simple notch in the upper lip to a complete opening in the lip extending into the floor of the nostril and involving the upper gum. ",
"keywords": null
},
{
"identifier": "Deafness, autosomal dominant, 10.",
"acronym": "DFNA10.",
"accession": "DI-00840",
"synonyms": "Non-syndromic neurosensory deafness autosomal dominant type 10.; Non-syndromic sensorineural deafness autosomal dominant type 10.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
},
{
"identifier": "Deafness, autosomal dominant, 13.",
"acronym": "DFNA13.",
"accession": "DI-00843",
"synonyms": "Non-syndromic neurosensory deafness autosomal dominant type 13.; Non-syndromic sensorineural deafness autosomal dominant type 13.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
},
{
"identifier": "Deafness, autosomal dominant, 22.",
"acronym": "DFNA22.",
"accession": "DI-00847",
"synonyms": "Non-syndromic neurosensory deafness autosomal dominant type 22.; Non-syndromic sensorineural deafness autosomal dominant type 22.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. DFNA22 is progressive and postlingual, with onset during childhood. By the age of approximately 50 years, affected individuals invariably have profound sensorineural deafness. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
},
{
"identifier": "Deafness, autosomal dominant, 25.",
"acronym": "DFNA25.",
"accession": "DI-00848",
"synonyms": "Non-syndromic neurosensory deafness autosomal dominant type 25.; Non-syndromic sensorineural deafness autosomal dominant type 25.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. DFNA25 expression is variable in terms of onset and rate of progression, with an age-dependent penetrance resembling an early-onset presbycusis, or senile deafness, a progressive bilateral loss of hearing that occurs in the aged. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
},
{
"identifier": "Deafness, autosomal dominant, 28.",
"acronym": "DFNA28.",
"accession": "DI-00849",
"synonyms": "Non-syndromic neurosensory deafness autosomal dominant type 28.; Non-syndromic sensorineural deafness autosomal dominant type 28.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. DFNA28 is characterized by mild to moderate hearing loss across most frequencies that progresses to severe loss in the higher frequencies by the fifth decade. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
},
{
"identifier": "Deafness, autosomal dominant, 2A.",
"acronym": "DFNA2A.",
"accession": "DI-00832",
"synonyms": "Non-syndromic neurosensory deafness autosomal dominant type 2A.; Non-syndromic sensorineural deafness autosomal dominant type 2A.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
},
{
"identifier": "Deafness, autosomal dominant, 36.",
"acronym": "DFNA36.",
"accession": "DI-00850",
"synonyms": "Non-syndromic neurosensory deafness autosomal dominant type 36.; Non-syndromic sensorineural deafness autosomal dominant type 36.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. DFNA36 is a bilateral hearing loss, and begins at 5-10 years of age. It progresses to profound deafness within 10-15 years. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
},
{
"identifier": "Deafness, autosomal dominant, 3A.",
"acronym": "DFNA3A.",
"accession": "DI-00834",
"synonyms": "Non-syndromic neurosensory deafness autosomal dominant type 3A.; Non-syndromic sensorineural deafness autosomal dominant type 3A.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
},
{
"identifier": "Deafness, autosomal dominant, 3B.",
"acronym": "DFNA3B.",
"accession": "DI-00835",
"synonyms": "Non-syndromic neurosensory deafness autosomal dominant type 3B.; Non-syndromic sensorineural deafness autosomal dominant type 3B.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss characterized by a variable phenotype, ranging from bilateral middle to high frequency hearing loss to profound sensorineural deafness. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
},
{
"identifier": "Deafness, autosomal dominant, 5.",
"acronym": "DFNA5.",
"accession": "DI-00837",
"synonyms": "Non-syndromic neurosensory deafness autosomal dominant type 5.; Non-syndromic sensorineural deafness autosomal dominant type 5.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
},
{
"identifier": "Deafness, autosomal dominant, 64.",
"acronym": "DFNA64.",
"accession": "DI-03231",
"synonyms": "Non-syndromic neurosensory deafness autosomal dominant type 64.; Non-syndromic sensorineural deafness autosomal dominant type 64.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
},
{
"identifier": "Deafness, autosomal recessive, 16.",
"acronym": "DFNB16.",
"accession": "DI-00863",
"synonyms": "Non-syndromic neurosensory deafness autosomal recessive type 16.; Non-syndromic sensorineural deafness autosomal recessive type 16.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
},
{
"identifier": "Deafness, autosomal recessive, 18A.",
"acronym": "DFNB18A.",
"accession": "DI-00864",
"synonyms": "Non-syndromic neurosensory deafness autosomal recessive type 18.; Non-syndromic sensorineural deafness autosomal recessive type 18.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
},
{
"identifier": "Deafness, autosomal recessive, 21.",
"acronym": "DFNB21.",
"accession": "DI-00865",
"synonyms": "Non-syndromic neurosensory deafness autosomal recessive type 21.; Non-syndromic sensorineural deafness autosomal recessive type 21.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
},
{
"identifier": "Deafness, autosomal recessive, 22.",
"acronym": "DFNB22.",
"accession": "DI-00866",
"synonyms": "Non-syndromic neurosensory deafness autosomal recessive type 22.; Non-syndromic sensorineural deafness autosomal recessive type 22.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
},
{
"identifier": "Deafness, autosomal recessive, 23.",
"acronym": "DFNB23.",
"accession": "DI-00867",
"synonyms": "Non-syndromic neurosensory deafness autosomal recessive type 23.; Non-syndromic sensorineural deafness autosomal recessive type 23.; ",
"cross_references": "MeSH; D006319.",
"definition": "A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. ",
"keywords": "KW-1010:Non-syndromic deafness.; "
}
]
}