PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 1; PFBMFT1 |
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PULMONARY FIBROSIS, IDIOPATHIC; IPF |
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PULMONARY HYPERTENSION, PRIMARY, 1; PPH1 |
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PUNCTATE PALMOPLANTAR KERATODERMA TYPE 1 |
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PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY |
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PYCNODYSOSTOSIS |
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PYLE DISEASE; PYL |
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PYLORIC STENOSIS, INFANTILE HYPERTROPHIC, 1; IHPS1 |
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PYOGENIC ARTHRITIS-PYODERMA GANGRENOSUM-ACNE SYNDROME |
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PYOGENIC STERILE ARTHRITIS, PYODERMA GANGRENOSUM, AND ACNE |
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PYRIDOXAMINE 5-PRIME-PHOSPHATE OXIDASE DEFICIENCY; PNPOD |
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PYRIDOXINE-DEPENDENT EPILEPSY |
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PYROPOIKILOCYTOSIS, HEREDITARY; HPP |
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PYRUVATE DEHYDROGENASE E1-ALPHA DEFICIENCY; PDHAD |
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PYRUVATE DEHYDROGENASE E3-BINDING PROTEIN DEFICIENCY; PDHXD |
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PYRUVATE DEHYDROGENASE PHOSPHATASE DEFICIENCY; PDHPD |
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QUEBEC PLATELET DISORDER; QPD |
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RADIN BLOOD GROUP ANTIGEN; RD |
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RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2; RUSAT2 |
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RAHMAN SYNDROME; RMNS |
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