multiple carboxylase deficiency
human disease
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multiple carboxylase deficiency
Summary
multiple carboxylase deficiency is a designated intractable/rare disease[1].
Key Facts
- multiple carboxylase deficiency's instance of is recorded as designated intractable/rare disease[2].
- multiple carboxylase deficiency's instance of is recorded as class of disease[3].
- multiple carboxylase deficiency is a type of carbohydrate metabolic disorder[4].
- multiple carboxylase deficiency is a type of amino acid metabolic disorder[5].
- multiple carboxylase deficiency is a type of classic organic aciduria[6].
- multiple carboxylase deficiency is a type of other metabolic disease with skin involvement[7].
- multiple carboxylase deficiency is a type of vitamin metabolic disorder[8].
- multiple carboxylase deficiency's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4825[9].
- multiple carboxylase deficiency's health specialty is recorded as medical genetics[10].
- multiple carboxylase deficiency's health specialty is recorded as endocrinology[11].
- multiple carboxylase deficiency's exact match is recorded as http://purl.obolibrary.org/obo/DOID_857[12].
- multiple carboxylase deficiency's exact match is recorded as http://identifiers.org/doid/DOID:857[13].
- multiple carboxylase deficiency's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_148[14].
- multiple carboxylase deficiency's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].