Conditions
Starting with Y
Private, moderated rooms - one per condition - with verified information and people who get it.
YAP1-MAMLD1 Fusion-Positive Supratentorial EpendymomaA supratentorial ependymoma that is caused by YAP1-MAMLD1 fusion.YawsA primary bacterial infectious disease that results in infection located in skin, located in joint or located in bone, is caused by Treponema pallidum subsp pertenue, which is transmitted by direct skin contact with an iYellow FeverA mosquito-borne viral infection causing jaundice.Yellow Nail SyndromeA 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 dystrophicY-Linked DeafnessA nonsyndromic deafness characterized by a Y-lnked inheritance mode.Y-Linked Deafness 1A Y-linked deafness characterized by male-limited postlingual progressive sensorineural hearing loss of variable severity, with onset in the first to third decades of life.Y-Linked Deafness 2A Y-linked deafness characterized by male-limited bilateral progressive sensorineural hearing loss of variable severity, with onset in the third to fifth decades of life that is caused by mutation in the TBL1Y gene on chY-Linked Monogenic DiseaseA monogenic disease that is caused by mutations on the Y chromosome.Y-Linked Spermatogenic Failure 1A Sertoli cell-only syndrome that is caused by deletions in the Yq11 chromosomal region.Y-Linked Spermatogenic Failure 2A spermatogenic failure that is characterized by nonobstroctive azoospermia or oligozoospermia that is caused by interstitial deletions on the Yq11.221 chromosomal region.Yoon-Bellen Neurodevelopmental SyndromeA syndrome characterized by onset in the first decade of highly variable neurodevelopmental phenotypes including global developmental delay, intellectual disability, seizures, hearing and visual problems, and ataxia thatYu-Kury Neurodevelopmental SyndromeAn autosomal dominant intellectual developmental disorder characterized by developmental delay, speech delay, motor delay, and intellectual disability that is caused by heterozygous mutation in the PSMC5 gene on chromosoYunis-Varon SyndromeA 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
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