Results 1 - 10 of 10 results
Disease |
Synonyms |
Description |
Articles |
Phenotypes |
yellow fever
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Yellow fever, sylvan; jungle yellow fever; Sylvati..
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Yellow fever, sylvan; jungle yellow fever; Sylvatic yellow fever; urban yellow fever
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A viral infectious disease that results_in infecti.. [+]
A viral infectious disease that results_in infection, has_material_basis_in Yellow fever virus, which is transmitted_by Aedes, transmitted_by Haemagogus, or transmitted_by Sabethes species of mosquitoes. The infection has_symptom fever, has_symptom muscle pain, has_symptom backache, has_symptom headache, has_symptom shivers, has_symptom loss of appetite, has_symptom jaundice, and has_symptom bleeding from the mouth, nose, eyes or stomach leading to vomitus containing blood.
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yaws
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Bouba; frambesia; frambesia tropica; frambosie; po..
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Bouba; frambesia; frambesia tropica; frambosie; polypapilloma tropicum; thymosis
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A primary bacterial infectious disease that result.. [+]
A primary bacterial infectious disease that results_in infection located_in skin, located_in joint or located_in bone, has_material_basis_in Treponema pallidum subsp pertenue, which is transmitted_by direct skin contact with an infected person. The infection has_symptom skin lesions.
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yellow nail syndrome
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A syndrome that is characterized by an accumulatio.. [+]
A syndrome that is characterized by an accumulation of protein-rich fluid (lymph) in the soft layers of tissue under the skin resulting in pleural effusions, lymphedema (due to lymphatic hypoplasia) and yellow dystrophic nails hat lack a cuticle, grow slowly, and are loose or detached.
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Y-linked disease
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A monogenic disease that has_material_basis_in mua.. [+]
A monogenic disease that has_material_basis_in muations on the Y chromosome.
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Yunis-Varon syndrome
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cleidocranial dysplasia with micrognathia, absent ..
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cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia; cleidocranial dysplasia-micrognathia-absent thumbs syndrome
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A syndrome characterized by skeletal defects, incl.. [+]
A syndrome characterized by skeletal defects, including cleidocranial dysplasia and digital anomalies, and severe neurologic involvement with neuronal loss. Enlarged cytoplasmic vacuoles are found in neurons, muscle, and cartilage. It is usually lethal in infancy and has material basis in homozygous or compound heterozygous mutation in the FIG4 gene on chromosome 6q21.
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endodermal sinus tumor
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Yolk Sac neoplasm; Yolk sac tumor; Hepatoid yolk s..
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Yolk sac tumor; Yolk Sac neoplasm; Hepatoid yolk sac tumour; infantile embryonal carcinoma
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A germ cell cancer that has_material_basis_in cell.. [+]
A germ cell cancer that has_material_basis_in cells that line the yolk sac of the embryo.
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central nervous system endodermal sinus tumor
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Yolk Sac tumor of the CNS; childhood central nervo..
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Yolk Sac tumor of the CNS; childhood central nervous system endodermal sinus neoplasm; pediatric central nervous system Yolk Sac tumor
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n_a
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cowpox
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yaba
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A viral infectious disease that results_in infecti.. [+]
A viral infectious disease that results_in infection in rodents, cows, and humans, located_in skin, has_material_basis_in Cowpox virus, which is transmitted_by contact with an infected animal. The infection results_in_formation_of vesicopustular lesions on the hands or face.
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late yaws
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Yaws gummata and ulcers (disorder); Gummata and ul..
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Yaws gummata and ulcers (disorder); Gummata and ulcers due to yaws; Gummata of yaws; gummatous frambeside; multiple papillomata due to yaws and wet crab yaws; nodular late yaws; nodular late yaws (disorder); Ulcers of yaws
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A yaws that appears after five years of the initia.. [+]
A yaws that appears after five years of the initial infection and is characterized by disabling consequences of the nose, bones and palmar/plantar hyperkeratosis.
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3-M syndrome
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Yakut short stature syndrome; dolichospondylic dys..
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Yakut short stature syndrome; dolichospondylic dysplasia; gloomy face syndrome; Le Merrer syndrome; Miller-McKusick-Malvaux syndrome; three M syndrome
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An autosomal recessive disease characterized by dw.. [+]
An autosomal recessive disease characterized by dwarfism, facial dysmorphia and skeletal abnormalities.
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