hereditary folate malabsorption

Summary

hereditary folate malabsorption is a hereditary disorder^[1].

Key Facts

• hereditary folate malabsorption's instance of is recorded as hereditary disorder^[2].
• hereditary folate malabsorption's instance of is recorded as designated intractable/rare disease^[3].
• hereditary folate malabsorption's instance of is recorded as rare disease^[4].
• hereditary folate malabsorption's instance of is recorded as class of disease^[5].
• hereditary folate malabsorption is a type of syndrome with combined immunodeficiency^[6].
• hereditary folate malabsorption is a type of vitamin metabolic disorder^[7].
• hereditary folate malabsorption is a type of disorder of folate metabolism and transport^[8].
• hereditary folate malabsorption is a type of metabolic disease with intestinal involvement^[9].
• hereditary folate malabsorption is a type of constitutional megaloblastic anemia due to folate metabolism disorder^[10].
• hereditary folate malabsorption is a type of intestinal disease due to vitamin absorption anomaly^[11].
• hereditary folate malabsorption is a type of autosomal recessive disease^[12].
• hereditary folate malabsorption's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4822^[13].
• hereditary folate malabsorption's has effect is recorded as folate deficiency^[14].
• hereditary folate malabsorption's NCI Thesaurus ID is recorded as C156424^[15].
• hereditary folate malabsorption's health specialty is recorded as medical genetics^[16].
• hereditary folate malabsorption's genetic association is recorded as SLC46A1^[17].
• hereditary folate malabsorption's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_90045^[18].
• hereditary folate malabsorption's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111678^[19].
• hereditary folate malabsorption's exact match is recorded as http://identifiers.org/doid/DOID:0111678^[20].