Trusted information across 10,888 rare diseases — plain language, always cited, free for everyone.
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Showing 8,961-8,980 of 10,888 diseases
MONDO:0020728
MONDO:0012793
MONDO:0010299
Hypoxanthine guanine phosphoribosyltransferase partial deficiency, also known as Kelley-Seegmiller syndrome, is a hereditary disorder of purine metabo...
MONDO:0016088
Hypoxanthine-guanine phosphoribosyltransferase deficiency is a hereditary disorder of purine metabolism characterized by an overproduction of uric aci...
MONDO:0034976
Information about the overall nature of iatrogenic Creutzfeldt-Jakob disease is currently limited for this condition. The condition is noted by its na...
MONDO:0005188
Iatrogenic Kaposi's sarcoma is a form of Kaposi's sarcoma that develops following organ transplantation or immunosuppressive treatment. It is consider...
MONDO:0016778
Iatrogenic botulism, also known as accidental or inadvertent botulism, is an acquired neuromuscular junction disorder resulting from the therapeutic o...
MONDO:0019845
Iatrogenic or traumatic pituitary deficiency is an endocrine condition that arises when the pituitary gland is damaged due to medical interventions or...
MONDO:0009440
MONDO:0019269
Ichthyosis is a group of disorders characterized by visible scaling and/or hyperkeratosis of the skin, primarily affecting keratinocyte differentiatio...
MONDO:0007809
Ichthyosis histrix, Lambert type is a rare skin condition that has been identified in various medical databases. It is known by several other names, i...
MONDO:0859383
Ichthyosis hystrix is a skin condition characterized by abnormal, thickened, and hyperkeratotic scaling of the skin. It is linked to genetic changes i...
MONDO:0007808
Ichthyosis hystrix of Curth-Macklin is a rare keratinopathic ichthyosis characterized primarily by severe hyperkeratotic skin lesions and marked palmo...
MONDO:0043106
MONDO:0012089
Ichthyosis prematurity syndrome is a rare congenital condition that primarily affects the skin and respiratory system. Infants with this syndrome are...
MONDO:0024304
MONDO:0957783
MONDO:0010223
Ichthyosis, X-linked, without steroid sulfatase deficiency is a skin condition that is characterized by abnormal skin scaling and dryness. Although it...
MONDO:0100303
Ichthyosis, annular epidermolytic 1 is a skin disorder characterized by annular epidermolytic ichthosis resulting from variations in the KRT10 gene. I...
MONDO:0859574
Ichthyosis, annular epidermolytic, 2 is a skin disorder primarily characterized by generalized ichthyosis and related skin changes. The condition is l...
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