Most common form of bowel obstruction in infancy
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DISO:OMIM |
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No skeletal abnormalities in odontohypophosphatasia
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DISO:OMIM |
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Hypertonia and rigidity during seizures
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DISO:OMIM |
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Susceptibility conferred by mutation in the butyrophilin-like protein 2 gene (BTNL2, 606000.0001)
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DISO:OMIM |
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PROSTATE CANCER, HEREDITARY, 9
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DISO:OMIM |
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Prostate Cancer, Hereditary, 9
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DISO:MSH |
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Direct care staff believe resident is capable of increased independence in at least some ADLs
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DISO:LNC |
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Osteoarthritis (hips, knees, shoulders, wrists, hands)
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DISO:OMIM |
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Caused by mutation in the mitochondrial tRNA lysine 1 gene (MTTL1, 590050.0001)
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DISO:OMIM |
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