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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Inherited thrombocytopenia
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Syndromic constitutional thrombocytopenia
DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome
rare
Identifiers
MONDO:0044635
Orphanet:494444
Part of
Syndromic constitutional thrombocytopenia
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