Condition

Alopecia Universalis

syndrome

ICD-10 L63.1

disease · Skin and Connective Tissue Diseases; Pathological Conditions, Signs and Symptoms

Alopecia Universalis Congenita

disease

disease · Skin and Connective Tissue Diseases; Pathological Conditions, Signs and Symptoms

Alopecia-Mental Retardation Syndrome 1

syndrome

disease · Mental Disorders; Nervous System Diseases; Behavior and Behavior Mechanisms; Skin and Connective Tissue Diseases; Pathological Conditions, Signs and Symptoms

Alopecia, Androgenetic, 1

syndrome

disease

Alopecia, Androgenetic, 2

syndrome

disease · Skin and Connective Tissue Diseases; Pathological Conditions, Signs and Symptoms

Alopecia, Androgenetic, 3

syndrome

disease · Skin and Connective Tissue Diseases; Pathological Conditions, Signs and Symptoms

Alopecia, Male Pattern

syndrome

disease · Skin and Connective Tissue Diseases; Pathological Conditions, Signs and Symptoms

Alopecia, Neurologic Defects, And Endocrinopathy Syndrome

syndrome

disease · Mental Disorders; Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms; Skin and Connective Tissue Diseases; Endocrine System Diseases

Alopecia, unspecified

disease

Alpers Syndrome (Disorder)

syndrome

disease · Immune System Diseases; Nervous System Diseases

Alpha 1-Antitrypsin Deficiency

syndrome

disease · Digestive System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Pathological Conditions, Signs and Symptoms

Alpha Carotene Level

phenotype

phenotype

Alpha Ketoadipic Aciduria

syndrome

disease

Alpha Thalassemia Intermedia

syndrome

disease

Alpha Thalassemia Minor

syndrome

disease

Alpha Trait Thalassemia

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases

Alpha^+^ Thalassemia

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases

Alpha^+^ Thalassemia, Deletion Type

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases

Alpha^0^ Thalassemia

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases

Alpha-1-Antitrypsin Deficiency, Autosomal Recessive

syndrome

disease · Digestive System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Pathological Conditions, Signs and Symptoms

Alpha-2-Antiplasmin Deficiency

syndrome

disease

Alpha-2-Macroglobulin Deficiency

syndrome

disease · Respiratory Tract Diseases

Alpha-2-Plasmin Inhibitor Deficiency

syndrome

disease · Hemic and Lymphatic Diseases

Alpha-Aminoadipic Aciduria

phenotype

phenotype

Alpha-Aminoadipic Semialdehyde Deficiency Disease

syndrome

disease · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases

Alpha-B Crystallinopathy

syndrome

disease · Cardiovascular Diseases; Eye Diseases; Nervous System Diseases; Musculoskeletal Diseases

Alpha-Dystroglycanopathies

syndrome

disease · Eye Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases

Alpha-Eeg

phenotype

phenotype

Alpha-Fetoprotein Deficiency

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases

Alpha-Fetoprotein, Hereditary Persistence Of

phenotype

phenotype

Alpha-Ketoglutarate Dehydrogenase Deficiency

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases

Alpha-L-Iduronidase Deficiency

syndrome

disease · Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases

Alpha-Mannosidosis

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases

Alpha-Methylacyl-Coa Racemase Deficiency

syndrome

disease · Nervous System Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases

Alpha-Sarcoglycanopathies

syndrome

disease · Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Respiratory Tract Diseases; Musculoskeletal Diseases

Alpha-Thalassemia

syndrome

ICD-10 D56.0

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases

Alpha-Thalassemia Mental Retardation Syndrome, Deletion-Type

syndrome

disease · Mental Disorders; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Behavior and Behavior Mechanisms; Pathological Conditions, Signs and Symptoms; Hemic and Lymphatic Diseases

Alpha-Thalassemia Myelodysplasia Syndrome

disease

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases

Alpha-Thalassemia-2, Nondeletional

disease

disease

Alpha-Thalassemia, Hmong Type

syndrome

disease

Alpha-Thalassemia/Mental Retardation Syndrome (301040) Is An Allelic Disorder

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases

Alpha-Thalassemia/Mental Retardation Syndrome, Nondeletion Type, X-Linked

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Hemic and Lymphatic Diseases

Alpha, Alpha-Trehalase Deficiency

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Pathological Conditions, Signs and Symptoms

Alpha/Beta T-Cell Lymphopenia With Gamma/Delta T-Cell Expansion, Severe Cytomegalovirus Infection, And Autoimmunity

syndrome

disease · Immune System Diseases; Infections; Hemic and Lymphatic Diseases

Alphaviral Infection

syndrome

disease

Alphavirus Infections

group

group · Infections

Alport Syndrome

syndrome

disease · Skin and Connective Tissue Diseases; Male Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications

Alport Syndrome 1, X-Linked

syndrome

disease