amino acid transport disorder
Human disease
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Summary
amino acid transport disorder is a class of disease[1]. It is known by 14 alternative names across languages and contexts.[2]
Key Facts
- Subclass of: congenital disorder of amino acid metabolism[3]
- ICD-9-CM: 270.0[4]
- Health specialty: medical genetics[5], endocrinology[6]
- Genetic association: HKDC1[7], GABRB1[8], ABCA4[9], AHR[10], AP3B2[11], ATP6V1A[12], BBS1[13], BBS2[14], CACNA1A[15], CACNA2D1[16], CNGA1[17], CRX[18], CTNS[19], CELF2[20]