Hemochromatosis, unspecified
E83.52 Hypercalcemia Notes: Familial hypocalciuric hypercalcemia
Hypercalcemia Notes: Familial hypocalciuric hypercalcemia
E85.2 Heredofamilial amyloidosis, unspecified
Heredofamilial amyloidosis, unspecified
E87.20 Acidosis, unspecified Notes: Lactic acidosis NOS ; Metabolic acidosis NOS
Acidosis, unspecified Notes: Lactic acidosis NOS ; Metabolic acidosis NOS
E88.02 Plasminogen deficiency Notes: Dysplasminogenemia ; Hypoplasminogenemia ; Type 1 plasminogen deficiency ; Type 2 plasmino…
Plasminogen deficiency Notes: Dysplasminogenemia ; Hypoplasminogenemia ; Type 1 plasminogen deficiency ; Type 2 plasminogen deficiency ; code for associated findings, such as: ; hydrocephalus (G91.4) ...
E74.3 Other disorders of intestinal carbohydrate absorption Notes: Disorder of intestinal carbohydrate absorption NOS ; Glucos…
Other disorders of intestinal carbohydrate absorption Notes: Disorder of intestinal carbohydrate absorption NOS ; Glucose-galactose malabsorption ; Sucrase deficiency ; lactose intolerance (E73.-)
E75.09 Other GM2 gangliosidosis Notes: Adult GM2 gangliosidosis ; Juvenile GM2 gangliosidosis
Other GM2 gangliosidosis Notes: Adult GM2 gangliosidosis ; Juvenile GM2 gangliosidosis
E75.249 Niemann-Pick disease, unspecified Notes: Acid sphingomyelinase deficiency (ASMD) NOS
Niemann-Pick disease, unspecified Notes: Acid sphingomyelinase deficiency (ASMD) NOS
