Human Disease List

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{
    "count": 6723,
    "next": null,
    "previous": "https://cinder.proteo.info/api/human_diseases/?format=api&limit=20&offset=6700&ordering=identifier",
    "results": [
        {
            "identifier": "Zimmermann-Laband syndrome 3.",
            "acronym": "ZLS3.",
            "accession": "DI-05702",
            "synonyms": null,
            "cross_references": "MeSH; D000015.",
            "definition": "A form of Zimmermann-Laband syndrome, a rare developmental disorder characterized by facial dysmorphism with bulbous nose and thick floppy ears, gingival enlargement, hypoplasia or aplasia of terminal phalanges and nails, hypertrichosis, joint hyperextensibility, and hepatosplenomegaly. Some patients manifest intellectual disability with or without epilepsy. ZLS3 inheritance is autosomal dominant. ",
            "keywords": null
        },
        {
            "identifier": "Zinc deficiency, transient neonatal.",
            "acronym": "TNZD.",
            "accession": "DI-03641",
            "synonyms": "Neonatal zinc deficiency due to low breast milk zinc.; ",
            "cross_references": "MeSH; D008664.",
            "definition": "A disorder occurring in breast-fed infants as a consequence of low milk zinc concentration in their nursing mothers, which cannot be corrected by maternal zinc supplementation. A large amount of zinc, an essential trace mineral, is required for normal growth particularly in infants, and breast milk normally contains adequate zinc to meet the requirement for infants up to 4 to 6 months of age. Zinc deficiency can lead to dermatitis, alopecia, decreased growth, and impaired immune function. The disorder shows autosomal dominant inheritance with incomplete penetrance. ",
            "keywords": null
        },
        {
            "identifier": "ZTTK syndrome.",
            "acronym": "ZTTKS.",
            "accession": "DI-04860",
            "synonyms": "Zhu-Tokita-Takenouchi-Kim syndrome.; ",
            "cross_references": "MeSH; D008607.",
            "definition": "An autosomal dominant syndrome characterized by intellectual disability, developmental delay, malformations of the cerebral cortex, epilepsy, vision problems, musculo-skeletal abnormalities, and congenital malformations. ",
            "keywords": "KW-0991:Intellectual disability.; "
        }
    ]
}