Browse By

Rare (Under 1 in 2000)

Facts
Comparison
ICD-10 Chapter Number
IV 1
ICD-10 Code Range
E00-E90 1
Rare (Under 1 in 2000)
Filter Results90 entries

Abetalipoproteinemia

Rare (Under 1 in 2000)

Aceruloplasminemia

Rare (Under 1 in 2000)

Acrodermatitis enteropathica

Rare (Under 1 in 2000)

Acromegaly

Rare (Under 1 in 2000)

Adenine phosphoribosyltransferase deficiency

Rare (Under 1 in 2000)

Adenylosuccinate lyase deficiency

Rare (Under 1 in 2000)

Adult polyglucosan body disease

Rare (Under 1 in 2000)

Alexander disease

Rare (Under 1 in 2000)

ALG1-CDG

Rare (Under 1 in 2000)

Alkaptonuria

Rare (Under 1 in 2000)

Alpha-mannosidosis

Rare (Under 1 in 2000)

Amyloidosis

Rare (Under 1 in 2000)

Argininemia

Rare (Under 1 in 2000)

Argininosuccinic aciduria

Rare (Under 1 in 2000)

Aromatase deficiency

Rare (Under 1 in 2000)

Aromatase excess syndrome

Rare (Under 1 in 2000)

Aspartylglucosaminuria

Rare (Under 1 in 2000)

Bartter syndrome

Rare (Under 1 in 2000)

Beta-ketothiolase deficiency

Rare (Under 1 in 2000)

Carbamoyl phosphate synthetase I deficiency

Rare (Under 1 in 2000)

Carnitine palmitoyltransferase II deficiency

Rare (Under 1 in 2000)

Cerebrotendinous xanthomatosis

Rare (Under 1 in 2000)

Chylomicron retention disease

Rare (Under 1 in 2000)

Congenital adrenal hyperplasia

Rare (Under 1 in 2000)

Congenital generalized lipodystrophy

Rare (Under 1 in 2000)

Crigler-Najjar syndrome

Rare (Under 1 in 2000)

Cystinosis

Rare (Under 1 in 2000)

Danon disease

Rare (Under 1 in 2000)

Donohue syndrome

Rare (Under 1 in 2000)

Fabry Disease

Rare (Under 1 in 2000)

Familial Amyloidosis, Finnish Type

Rare (Under 1 in 2000)

Farber disease

Rare (Under 1 in 2000)

Fumarase deficiency

Rare (Under 1 in 2000)

Galactosemia

Rare (Under 1 in 2000)

Galactosialidosis

Rare (Under 1 in 2000)

Gaucher Disease

Rare (Under 1 in 2000)

Glutaric aciduria type 1

Rare (Under 1 in 2000)

Glycogen storage disease type I

Rare (Under 1 in 2000)

Glycogen storage disease type IV

Rare (Under 1 in 2000)

Hartnup disease

Rare (Under 1 in 2000)

Hereditary fructose intolerance

Rare (Under 1 in 2000)

Hermansky-Pudlak syndrome

Rare (Under 1 in 2000)

Hunter syndrome

Rare (Under 1 in 2000)

Hutchinson-Gilford Progeria Syndrome

Rare (Under 1 in 2000)

Hypophosphatasia

Rare (Under 1 in 2000)

Isovaleric acidemia

Rare (Under 1 in 2000)

Laron syndrome

Rare (Under 1 in 2000)

Lecithin cholesterol acyltransferase deficiency

Rare (Under 1 in 2000)

Lesch-Nyhan syndrome

Rare (Under 1 in 2000)

Leydig cell hypoplasia

Rare (Under 1 in 2000)

Showing 1 to 50 of 90, page 1 of 2.

Sources
1. ICD-10 (Wikipedia)
  • ICD-10 chapter table, Chapter IV, chapter number
    IV | E00-E90 | "Endocrine, nutritional and metabolic diseases"
  • ICD-10 chapter table, Chapter IV, code range
    IV | E00-E90 | "Endocrine, nutritional and metabolic diseases"
Comments (0)
No comments yet. Be the first to share a thought.
Reader Challenges (0)
No disputes yet. Spotted an error or a better source? Open the first one.

Medicine Atlas

How Healing Is Practiced
Sign In
Text size
100%
Theme