A A A+ A- A0 A1 A2 A3 A4 A5 A6 A7 A8 A9 AA AB AC AD AE AF AG AH AI AJ AK AL AM AN AO AP AQ AR AS AT AU AV AW AX AY AZ
acrodermatitis enteropathica
[severe human skin and gastrointestinal disease inherited as a recessive autosomal trait that is characterized by the symptoms of zinc deficiency and clears up when zinc is added to the diet. ( CSP )]
UMLS (CSP) C0221036- Disease or Syndrome
Relation/PAR: Genetic Condition
Congenital anomalies of the integument
congenital gastrointestinal disorder
Congenital anomalies of the integument
congenital gastrointestinal disorder
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