hawkinsinuria
disease
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hawkinsinuria
Summary
hawkinsinuria is a rare disease[1].
Key Facts
- hawkinsinuria's instance of is recorded as rare disease[2].
- hawkinsinuria's instance of is recorded as class of disease[3].
- hawkinsinuria is a type of tyrosinemia[4].
- hawkinsinuria is a type of amino acid metabolic disorder[5].
- hawkinsinuria is a type of autosomal dominant disease[6].
- hawkinsinuria's health specialty is recorded as endocrinology[7].
- hawkinsinuria's genetic association is recorded as HPD[8].
- hawkinsinuria's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2118[9].
- hawkinsinuria's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111362[10].
- hawkinsinuria's exact match is recorded as http://identifiers.org/doid/DOID:0111362[11].