Diseases

Explore disease pages that summarize symptoms, diagnostic context, and related care topics.

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All diseases (73,990)

E639

Nutritional deficiency, unspecified

E640

Sequelae of protein-calorie malnutrition

E641

Sequelae of vitamin A deficiency

E642

Sequelae of vitamin C deficiency

E643

Sequelae of rickets

E648

Sequelae of other nutritional deficiencies

E649

Sequelae of unspecified nutritional deficiency

E6601

Morbid (severe) obesity due to excess calories

E6609

Other obesity due to excess calories

E661

Drug-induced obesity

E662

Morbid (severe) obesity with alveolar hypoventilation

E66811

Obesity, class 1

E66812

Obesity, class 2

E66813

Obesity, class 3

E6689

Other obesity not elsewhere classified

E669

Obesity, unspecified

E670

Hypervitaminosis A

E671

Hypercarotenemia

E672

Megavitamin-B6 syndrome

E673

Hypervitaminosis D

E678

Other specified hyperalimentation

E700

Classical phenylketonuria

E701

Other hyperphenylalaninemias

E7020

Disorder of tyrosine metabolism, unspecified

E7021

Tyrosinemia

E7029

Other disorders of tyrosine metabolism

E7030

Albinism, unspecified

E70310

X-linked ocular albinism

E70311

Autosomal recessive ocular albinism

E70318

Other ocular albinism

E70319

Ocular albinism, unspecified

E70320

Tyrosinase negative oculocutaneous albinism

E70321

Tyrosinase positive oculocutaneous albinism

E70328

Other oculocutaneous albinism

E70329

Oculocutaneous albinism, unspecified

E70330

Chediak-Higashi syndrome

E70331

Hermansky-Pudlak syndrome

E70338

Other albinism with hematologic abnormality

E70339

Albinism with hematologic abnormality, unspecified

E7039

Other specified albinism

E7040

Disorders of histidine metabolism, unspecified

E7041

Histidinemia

E7049

Other disorders of histidine metabolism

E705

Disorders of tryptophan metabolism

E7081

Aromatic L-amino acid decarboxylase deficiency

E7089

Other disorders of aromatic amino-acid metabolism

E709

Disorder of aromatic amino-acid metabolism, unspecified

E710

Maple-syrup-urine disease

E71110

Isovaleric acidemia

E71111

3-methylglutaconic aciduria

E71118

Other branched-chain organic acidurias

E71120

Methylmalonic acidemia

E71121

Propionic acidemia

E71128

Other disorders of propionate metabolism

E7119

Other disorders of branched-chain amino-acid metabolism

E712

Disorder of branched-chain amino-acid metabolism, unspecified

E7130

Disorder of fatty-acid metabolism, unspecified

E71310

Long chain/very long chain acyl CoA dehydrogenase deficiency

E71311

Medium chain acyl CoA dehydrogenase deficiency

E71312

Short chain acyl CoA dehydrogenase deficiency

E71313

Glutaric aciduria type II

E71314

Muscle carnitine palmitoyltransferase deficiency

E71318

Other disorders of fatty-acid oxidation

E7132

Disorders of ketone metabolism

E7139

Other disorders of fatty-acid metabolism

E7140

Disorder of carnitine metabolism, unspecified

E7141

Primary carnitine deficiency

E7142

Carnitine deficiency due to inborn errors of metabolism

E7143

Iatrogenic carnitine deficiency

E71440

Ruvalcaba-Myhre-Smith syndrome

E71448

Other secondary carnitine deficiency

E7150

Peroxisomal disorder, unspecified

E71510

Zellweger syndrome

E71511

Neonatal adrenoleukodystrophy

E71518

Other disorders of peroxisome biogenesis

E71520

Childhood cerebral X-linked adrenoleukodystrophy

E71521

Adolescent X-linked adrenoleukodystrophy

E71522

Adrenomyeloneuropathy

E71528

Other X-linked adrenoleukodystrophy

E71529

X-linked adrenoleukodystrophy, unspecified type

E7153

Other group 2 peroxisomal disorders

E71540

Rhizomelic chondrodysplasia punctata

E71541

Zellweger-like syndrome

E71542

Other group 3 peroxisomal disorders

E71548

Other peroxisomal disorders

E7200

Disorders of amino-acid transport, unspecified

E7201

Cystinuria

E7202

Hartnup's disease

E7203

Lowe's syndrome

E7204

Cystinosis

E7209

Other disorders of amino-acid transport

E7210

Disorders of sulfur-bearing amino-acid metabolism, unspecified

E7211

Homocystinuria

E7212

Methylenetetrahydrofolate reductase deficiency

E7219

Other disorders of sulfur-bearing amino-acid metabolism

E7220

Disorder of urea cycle metabolism, unspecified

E7221

Argininemia

E723

Disorders of lysine and hydroxylysine metabolism

E724

Disorders of ornithine metabolism

L811

Chloasma