Human Disease List
GET /api/human_diseases/?format=api&offset=1020&ordering=-identifier
{ "count": 6723, "next": "https://cinder.proteo.info/api/human_diseases/?format=api&limit=20&offset=1040&ordering=-identifier", "previous": "https://cinder.proteo.info/api/human_diseases/?format=api&limit=20&offset=1000&ordering=-identifier", "results": [ { "identifier": "Retinitis pigmentosa 86.", "acronym": "RP86.", "accession": "DI-05674", "synonyms": null, "cross_references": "MeSH; D012174.", "definition": "A form of retinitis pigmentosa, 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. RP86 is an autosomal recessive form. ", "keywords": "KW-0682:Retinitis pigmentosa.; " }, { "identifier": "Retinitis pigmentosa 85.", "acronym": "RP85.", "accession": "DI-05496", "synonyms": null, "cross_references": "MeSH; D012174.", "definition": "A form of retinitis pigmentosa, 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. RP85 is an autosomal recessive form manifesting as early-onset progressive difficulty to adapt in dim light and gradually decreasing visual acuity in both eyes. ", "keywords": "KW-0682:Retinitis pigmentosa.; " }, { "identifier": "Retinitis pigmentosa 84.", "acronym": "RP84.", "accession": "DI-05397", "synonyms": null, "cross_references": "MeSH; D012174.", "definition": "A form of retinitis pigmentosa, 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. RP84 is an autosomal recessive, early onset form characterized by night blindness by age 4 and complete blindness by age 8. Funduscopy shows severely attenuated retinal vessels, severe macular atrophy, and prominent and deep macular colobomas lacking neuroretinal tissue. ", "keywords": "KW-0682:Retinitis pigmentosa.; " }, { "identifier": "Retinitis pigmentosa 83.", "acronym": "RP83.", "accession": "DI-05372", "synonyms": null, "cross_references": "MeSH; D012174.", "definition": "An autosomal dominant form of retinitis pigmentosa, 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": null }, { "identifier": "Retinitis pigmentosa 82 with or without situs inversus.", "acronym": "RP82.", "accession": "DI-03887", "synonyms": null, "cross_references": "MeSH; D012857.", "definition": "An autosomal recessive disorder characterized by variable association of retinitis pigmentosa with situs inversus. 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. Situs inversus is a congenital abnormality in which organs in the thorax and the abdomen are opposite to their normal positions due to lateral transposition. ", "keywords": "KW-1186:Ciliopathy.; " }, { "identifier": "Retinitis pigmentosa 81.", "acronym": "RP81.", "accession": "DI-05187", "synonyms": null, "cross_references": "MeSH; D012174.", "definition": "A form of retinitis pigmentosa, 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. RP81 inheritance is autosomal recessive. ", "keywords": "KW-0682:Retinitis pigmentosa.; " }, { "identifier": "Retinitis pigmentosa 80.", "acronym": "RP80.", "accession": "DI-05130", "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. RP80 inheritance is autosomal recessive. ", "keywords": "KW-0682:Retinitis pigmentosa.; " }, { "identifier": "Retinitis pigmentosa 79.", "acronym": "RP79.", "accession": "DI-04983", "synonyms": null, "cross_references": "MeSH; D012174.", "definition": "A form of retinitis pigmentosa, 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. RP79 inheritance is autosomal dominant. ", "keywords": "KW-0682:Retinitis pigmentosa.; " }, { "identifier": "Retinitis pigmentosa 78.", "acronym": "RP78.", "accession": "DI-04985", "synonyms": null, "cross_references": "MeSH; D012174.", "definition": "A form of retinitis pigmentosa, 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. RP78 inheritance is autosomal recessive. ", "keywords": "KW-0682:Retinitis pigmentosa.; " }, { "identifier": "Retinitis pigmentosa 77.", "acronym": "RP77.", "accession": "DI-04926", "synonyms": null, "cross_references": "MeSH; D012174.", "definition": "A form of retinitis pigmentosa, 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. RP77 inheritance is autosomal recessive. ", "keywords": "KW-0682:Retinitis pigmentosa.; " }, { "identifier": "Retinitis pigmentosa 76.", "acronym": "RP76.", "accession": "DI-04824", "synonyms": null, "cross_references": "MeSH; D012174.", "definition": "A form of retinitis pigmentosa, 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. RP76 inheritance is autosomal recessive. ", "keywords": "KW-0682:Retinitis pigmentosa.; " }, { "identifier": "Retinitis pigmentosa 75.", "acronym": "RP75.", "accession": "DI-04756", "synonyms": null, "cross_references": "MeSH; D012174.", "definition": "A form of retinitis pigmentosa, 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. RP75 inheritance is autosomal recessive. ", "keywords": "KW-0682:Retinitis pigmentosa.; " }, { "identifier": "Retinitis pigmentosa 74.", "acronym": "RP74.", "accession": "DI-04520", "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": "Retinitis pigmentosa 73.", "acronym": "RP73.", "accession": "DI-04519", "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": "Retinitis pigmentosa 72.", "acronym": "RP72.", "accession": "DI-04485", "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": "Retinitis pigmentosa 71.", "acronym": "RP71.", "accession": "DI-04435", "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": "Retinitis pigmentosa 70.", "acronym": "RP70.", "accession": "DI-04177", "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": "Retinitis pigmentosa 7.", "acronym": "RP7.", "accession": "DI-00975", "synonyms": "Retinitis pigmentosa 7 digenic.; ", "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": "Retinitis pigmentosa 69.", "acronym": "RP69.", "accession": "DI-04068", "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": "Retinitis pigmentosa 68.", "acronym": "RP68.", "accession": "DI-04064", "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.; " } ] }