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"name": "inborn errors of metabolism",
"definition": "['\"A simple genetic disease that comprises a large class of genetic diseases involving disorders of metabolism.\" [url:http\\\\://en.wikipedia.org/wiki/Inborn_errors_of_metabolism]']",
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"accession": "DOID:654",
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"accession": "DOID:6536",
"name": "plasma cell neoplasm",
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"name": "inborn errors purine-pyrimidine metabolism",
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"name": "congenital musculoskeletal abnormality",
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"accession": "DOID:65",
"name": "connective tissue disease",
"definition": "['A musculoskeletal system disease that affects tissues such as skin, tendons, and cartilage.']",
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"accession": "DOID:649",
"name": "prion disease",
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"accession": "DOID:6486",
"name": "skin and subcutaneous tissue disease",
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"accession": "DOID:6457",
"name": "Lhermitte-Duclos disease",
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"accession": "DOID:6420",
"name": "pulmonary valve stenosis",
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"name": "tetralogy of Fallot",
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"accession": "DOID:641",
"name": "CNS demyelinating autoimmune disease",
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"accession": "DOID:638",
"name": "demyelinating disease of central nervous system",
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"name": "metabolic brain disease",
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"name": "hereditary disease",
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"name": "congenital disorder of natural immunity",
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"accession": "DOID:628",
"name": "combined T cell and B cell immunodeficiency",
"definition": "[]",
"term_type": "cell line"
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"accession": "DOID:627",
"name": "severe combined immunodeficiency",
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"accession": "DOID:620",
"name": "blood protein disorder",
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