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https://ai.google.dev/competition/projects/medgen?hl=pl Medgen, | Gemini API Developer Competition | Google AI for Developers System wsparcia klinicznego gemini apigoogle aimedgendevelopercompetition https://www.ncbi.nlm.nih.gov/medgen/42391 Hemeralopia (Concept Id: C0018975) - MedGen - NCBI A visual defect characterized by the inability to see as clearly in bright light as in dim light. The word hemeralopia literally means day blindness. hemeralopiaconceptidmedgenncbi https://www.ncbi.nlm.nih.gov/medgen/?cmd=HTOn& Error - MedGen - NCBI errormedgenncbi https://www.ncbi.nlm.nih.gov/medgen/137994 Diaper candidiasis (Concept Id: C0343874) - MedGen - NCBI An inflammatory skin condition in the diaper area superimposed with Candida infection, characterized by a bright red rash with a sharply demarcated edge and... diaper candidiasisconceptmedgenncbi https://www.ncbi.nlm.nih.gov/medgen/C1861689 Klippel-Feil syndrome 1, autosomal dominant (Concept Id: C1861689) - MedGen - NCBI Klippel-Feil syndrome is a bone disorder that is characterized by the abnormal joining (fusion) of two or more spinal bones in the neck (cervical vertebrae).... klippel feil syndromeautosomal dominant1 https://www.ncbi.nlm.nih.gov/medgen/508423 Senile purpura (Concept Id: C0149766) - MedGen - NCBI senile purpuraconceptidmedgenncbi https://www.ncbi.nlm.nih.gov/medgen/8524 Ecchymosis (Concept Id: C0013491) - MedGen - NCBI A purpuric lesion that is larger than 1 cm in diameter. ecchymosisconceptidmedgenncbi https://www.ncbi.nlm.nih.gov/medgen/C3661900 not provided (Concept Id: C3661900) - MedGen - NCBI The term 'not provided' is registered in MedGen to support identification of submissions to ClinVar for which no condition was named when assessing the... not providedconceptmedgenncbi https://www.ncbi.nlm.nih.gov/medgen/353402 B-Symptoms (Concept Id: C1706867) - MedGen - NCBI Features commonly associated with lymphoma, including fever above 38C, drenching night sweats, and weight loss of more than 10% of body mass in the previous 6... b symptomsconceptidmedgenncbi https://www.ncbi.nlm.nih.gov/medgen/333014 ABCD syndrome (Concept Id: C1838099) - MedGen - NCBI ABCD syndrome (ABCDS) is an autosomal recessive disorder characterized by albinism, black lock, cell migration disorder of the neurocytes of the gut... abcd syndromeconceptidmedgenncbi https://www.ncbi.nlm.nih.gov/medgen/C3715164 Leber congenital amaurosis 17 (Concept Id: C3715164) - MedGen - NCBI At least 20 genetic types of Leber congenital amaurosis have been described. The types are distinguished by their genetic cause, patterns of vision loss, and... leber congenital amaurosis17conceptidmedgen https://www.ncbi.nlm.nih.gov/medgen/CN517202 not provided (Concept Id: C3661900) - MedGen - NCBI The term 'not provided' is registered in MedGen to support identification of submissions to ClinVar for which no condition was named when assessing the... not providedconceptmedgenncbi https://ai.google.dev/competition/projects/medgen?hl=it Medgen | Gemini API Developer Competition | Google AI for Developers Sistema di assistenza clicinale gemini apigoogle aimedgendevelopercompetition https://drive.google.com/file/d/1xla8WjcOuhocYc-DB7U17pMn7TvhR5Vk/view?usp=sharing 2023-07-28 Mondo Outreach Call - MedGen.mp4 - Google Drive 20230728mondooutreach https://www.medgen.uzh.ch/de.html MEDGEN | Institut für Medizinische Genetik | UZH Das Institut für Medizinische Genetik der Universität Zürich engagiert sich sowohl in Forschung und Lehre als auch in der Dienstleistung für Patienten mit... medgeninstitutmedizinischegenetikuzh https://portal.medgenehr.com/medgenweb/ Medgen EHR Portal medgenehrportal https://www.ncbi.nlm.nih.gov/medgen/75778 Thrombocytopenia due to immune destruction (Concept Id: C0272286) - MedGen - NCBI Thrombocytopenia that results from immune destruction of platelets. due tothrombocytopeniaimmunedestructionconcept