alpha-aminoadipic and alpha-ketoadipic aciduria
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alpha-aminoadipic and alpha-ketoadipic aciduria
Summary
alpha-aminoadipic and alpha-ketoadipic aciduria is a rare disease[1]. It is known by 7 alternative names across languages and contexts.[2]
Key Facts
- alpha-aminoadipic and alpha-ketoadipic aciduria's instance of is recorded as rare disease[3].
- alpha-aminoadipic and alpha-ketoadipic aciduria's instance of is recorded as class of disease[4].
- alpha-aminoadipic and alpha-ketoadipic aciduria is a type of Ketoadipicaciduria[5].
- alpha-aminoadipic and alpha-ketoadipic aciduria is a type of disorder of lysine and hydroxylysine metabolism[6].
- alpha-aminoadipic and alpha-ketoadipic aciduria is a type of autosomal recessive disease[7].
- alpha-aminoadipic and alpha-ketoadipic aciduria is a type of amino acid metabolic disorder[8].
- alpha-aminoadipic and alpha-ketoadipic aciduria's genetic association is recorded as DHTKD1[9].
- alpha-aminoadipic and alpha-ketoadipic aciduria's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_79154[10].
- alpha-aminoadipic and alpha-ketoadipic aciduria's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111453[11].
- alpha-aminoadipic and alpha-ketoadipic aciduria's exact match is recorded as http://identifiers.org/doid/DOID:0111453[12].
Why It Matters
alpha-aminoadipic and alpha-ketoadipic aciduria is known by 7 alternative names across languages and contexts.[2]