Human Disease List
GET /api/human_diseases/?format=api&offset=5960&ordering=-identifier
{ "count": 6723, "next": "https://cinder.proteo.info/api/human_diseases/?format=api&limit=20&offset=5980&ordering=-identifier", "previous": "https://cinder.proteo.info/api/human_diseases/?format=api&limit=20&offset=5940&ordering=-identifier", "results": [ { "identifier": "Cardiomyopathy, dilated, 1II.", "acronym": "CMD1II.", "accession": "DI-03750", "synonyms": null, "cross_references": "MeSH; D002311.", "definition": "A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. ", "keywords": "KW-0122:Cardiomyopathy.; " }, { "identifier": "Cardiomyopathy, dilated, 1I.", "acronym": "CMD1I.", "accession": "DI-00216", "synonyms": null, "cross_references": "MeSH; D002311.", "definition": "A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. ", "keywords": "KW-0122:Cardiomyopathy.; " }, { "identifier": "Cardiomyopathy, dilated, 1HH.", "acronym": "CMD1HH.", "accession": "DI-03042", "synonyms": null, "cross_references": "MeSH; D002311.", "definition": "A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. ", "keywords": "KW-0122:Cardiomyopathy.; " }, { "identifier": "Cardiomyopathy, dilated, 1GG.", "acronym": "CMD1GG.", "accession": "DI-02945", "synonyms": null, "cross_references": "MeSH; D002311.", "definition": "A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. ", "keywords": "KW-0122:Cardiomyopathy.; " }, { "identifier": "Cardiomyopathy, dilated, 1G.", "acronym": "CMD1G.", "accession": "DI-00215", "synonyms": null, "cross_references": "MeSH; D002311.", "definition": "A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. ", "keywords": "KW-0122:Cardiomyopathy.; " }, { "identifier": "Cardiomyopathy, dilated, 1FF.", "acronym": "CMD1FF.", "accession": "DI-02681", "synonyms": null, "cross_references": "MeSH; D002311.", "definition": "A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. ", "keywords": "KW-0122:Cardiomyopathy.; " }, { "identifier": "Cardiomyopathy, dilated, 1EE.", "acronym": "CMD1EE.", "accession": "DI-02682", "synonyms": null, "cross_references": "MeSH; D002311.", "definition": "A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. ", "keywords": "KW-0122:Cardiomyopathy.; " }, { "identifier": "Cardiomyopathy, dilated, 1E.", "acronym": "CMD1E.", "accession": "DI-00214", "synonyms": "CDCD2.; Dilated cardiomyopathy with conduction defect 2.; Dilated cardiomyopathy with conduction disorder and arrhythmia.; ", "cross_references": "MeSH; D002311.", "definition": "A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. ", "keywords": "KW-0122:Cardiomyopathy.; " }, { "identifier": "Cardiomyopathy, dilated, 1DD.", "acronym": "CMD1DD.", "accession": "DI-02568", "synonyms": null, "cross_references": "MeSH; D002311.", "definition": "A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. ", "keywords": "KW-0122:Cardiomyopathy.; " }, { "identifier": "Cardiomyopathy, dilated, 1D.", "acronym": "CMD1D.", "accession": "DI-00213", "synonyms": null, "cross_references": "MeSH; D002311.", "definition": "A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. ", "keywords": "KW-0122:Cardiomyopathy.; " }, { "identifier": "Cardiomyopathy, dilated, 1C, with or without left ventricular non-compaction.", "acronym": "CMD1C.", "accession": "DI-00212", "synonyms": "Cardiomyopathy dilated with left ventricular noncompaction.; ", "cross_references": "MeSH; D002311.", "definition": "A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. Cardiomyopathy dilated type 1C is associated with left ventricular non-compaction in some patients. Left ventricular non-compaction is characterized by numerous prominent trabeculations and deep intertrabecular recesses in hypertrophied and hypokinetic segments of the left ventricle. ", "keywords": "KW-0122:Cardiomyopathy.; " }, { "identifier": "Cardiomyopathy, dilated, 1CC.", "acronym": "CMD1CC.", "accession": "DI-02530", "synonyms": null, "cross_references": "MeSH; D002311.", "definition": "A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. ", "keywords": "KW-0122:Cardiomyopathy.; " }, { "identifier": "Cardiomyopathy, dilated, 1BB.", "acronym": "CMD1BB.", "accession": "DI-02483", "synonyms": null, "cross_references": "MeSH; D002311.", "definition": "A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. ", "keywords": "KW-0122:Cardiomyopathy.; " }, { "identifier": "Cardiomyopathy, dilated, 1AA, with or without left ventricular non-compaction.", "acronym": "CMD1AA.", "accession": "DI-00211", "synonyms": null, "cross_references": "MeSH; D002311.", "definition": "A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. ", "keywords": "KW-0122:Cardiomyopathy.; " }, { "identifier": "Cardiomyopathy, dilated, 1A.", "acronym": "CMD1A.", "accession": "DI-00210", "synonyms": "Cardiomyopathy dilated with conduction defect 1.; CDCD1.; ", "cross_references": "MeSH; D002311.", "definition": "A disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. ", "keywords": "KW-0122:Cardiomyopathy.; " }, { "identifier": "Cardiofacioneurodevelopmental syndrome.", "acronym": "CFNDS.", "accession": "DI-05989", "synonyms": null, "cross_references": "MeSH; D000015.", "definition": "An autosomal recessive disorder characterized by global developmental delay, feeding difficulties, microcephaly and dysmorphic features. Additional features include cleft lip, cleft palate, variable cardiac defects, and abdominal situs inversus with asplenia. Brain imaging reveals cerebellar hypoplasia. ", "keywords": "KW-1186:Ciliopathy.; " }, { "identifier": "Cardiofaciocutaneous syndrome 4.", "acronym": "CFC4.", "accession": "DI-03781", "synonyms": null, "cross_references": "MeSH; D006330.", "definition": "A form of cardiofaciocutaneous syndrome, a multiple congenital anomaly disorder characterized by a distinctive facial appearance, heart defects and intellectual disability. Heart defects include pulmonic stenosis, atrial septal defects and hypertrophic cardiomyopathy. Some affected individuals present with ectodermal abnormalities such as sparse, friable hair, hyperkeratotic skin lesions and a generalized ichthyosis-like condition. Typical facial features are similar to Noonan syndrome. They include high forehead with bitemporal constriction, hypoplastic supraorbital ridges, downslanting palpebral fissures, a depressed nasal bridge, and posteriorly angulated ears with prominent helices. ", "keywords": "KW-0038:Ectodermal dysplasia.; KW-0122:Cardiomyopathy.; KW-0991:Intellectual disability.; " }, { "identifier": "Cardiofaciocutaneous syndrome 3.", "acronym": "CFC3.", "accession": "DI-03780", "synonyms": null, "cross_references": "MeSH; D006330.", "definition": "A form of cardiofaciocutaneous syndrome, a multiple congenital anomaly disorder characterized by a distinctive facial appearance, heart defects and intellectual disability. Heart defects include pulmonic stenosis, atrial septal defects and hypertrophic cardiomyopathy. Some affected individuals present with ectodermal abnormalities such as sparse, friable hair, hyperkeratotic skin lesions and a generalized ichthyosis-like condition. Typical facial features are similar to Noonan syndrome. They include high forehead with bitemporal constriction, hypoplastic supraorbital ridges, downslanting palpebral fissures, a depressed nasal bridge, and posteriorly angulated ears with prominent helices. Distinctive features of CFC3 include macrostomia and horizontal shape of palpebral fissures. ", "keywords": "KW-0038:Ectodermal dysplasia.; KW-0122:Cardiomyopathy.; KW-0991:Intellectual disability.; " }, { "identifier": "Cardiofaciocutaneous syndrome 2.", "acronym": "CFC2.", "accession": "DI-03779", "synonyms": null, "cross_references": "MeSH; D006330.", "definition": "A form of cardiofaciocutaneous syndrome, a multiple congenital anomaly disorder characterized by a distinctive facial appearance, heart defects and intellectual disability. Heart defects include pulmonic stenosis, atrial septal defects and hypertrophic cardiomyopathy. Some affected individuals present with ectodermal abnormalities such as sparse, friable hair, hyperkeratotic skin lesions and a generalized ichthyosis-like condition. Typical facial features are similar to Noonan syndrome. They include high forehead with bitemporal constriction, hypoplastic supraorbital ridges, downslanting palpebral fissures, a depressed nasal bridge, and posteriorly angulated ears with prominent helices. CFC2 patients often do not have the skin abnormalities, such as ichthyosis, hyperkeratosis, and hemangioma observed in CFC1. ", "keywords": "KW-0038:Ectodermal dysplasia.; KW-0122:Cardiomyopathy.; KW-0991:Intellectual disability.; " }, { "identifier": "Cardiofaciocutaneous syndrome 1.", "acronym": "CFC1.", "accession": "DI-01318", "synonyms": "Cardio-facio-cutaneous syndrome.; CFCS.; CFC syndrome.; ", "cross_references": "MeSH; D006330.", "definition": "A multiple congenital anomaly disorder characterized by a distinctive facial appearance, heart defects and intellectual disability. Heart defects include pulmonic stenosis, atrial septal defects and hypertrophic cardiomyopathy. Some affected individuals present with ectodermal abnormalities such as sparse, friable hair, hyperkeratotic skin lesions and a generalized ichthyosis-like condition. Typical facial features are similar to Noonan syndrome. They include high forehead with bitemporal constriction, hypoplastic supraorbital ridges, downslanting palpebral fissures, a depressed nasal bridge, and posteriorly angulated ears with prominent helices. ", "keywords": "KW-0038:Ectodermal dysplasia.; KW-0122:Cardiomyopathy.; KW-0991:Intellectual disability.; " } ] }