Condition

Apolipoprotein A-I (Giessen) Phenotype

phenotype

phenotype

Apolipoprotein A-I (Marburg) Phenotype

phenotype

phenotype

Apolipoprotein A-I (Milano) Phenotype

phenotype

phenotype

Apolipoprotein A-I (Munster3B) Phenotype

phenotype

phenotype

Apolipoprotein A-I (Munster3C) Phenotype

phenotype

phenotype

Apolipoprotein A-I (Munster4) Phenotype

phenotype

phenotype

Apolipoprotein A-I (Norway) Phenotype

phenotype

phenotype

Apolipoprotein A-I Deficiency

phenotype

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

Apolipoprotein A-Iv Polymorphism, Apoa4*1/Apoa4*2 Phenotype

phenotype

phenotype

Apolipoprotein B Assay

phenotype

phenotype

Apolipoprotein C-Ii (Auckland) Phenotype

phenotype

phenotype

Apolipoprotein C-Ii (Bari) Phenotype

phenotype

phenotype

Apolipoprotein C-Ii (Padova) Phenotype

phenotype

phenotype

Apolipoprotein C-Ii (Paris) Phenotype

phenotype

phenotype

Apolipoprotein C-Ii (San Francisco)

phenotype

phenotype

Apolipoprotein C-Ii (Wakayama) Phenotype

phenotype

phenotype

Apolipoprotein C-Ii Deficiency (Disorder)

syndrome

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

Apolipoprotein C-Ii Variant Phenotype

phenotype

phenotype

Apolipoprotein C-Iii Deficiency

syndrome

disease · Nutritional and Metabolic Diseases

Apolipoprotein C-Iii, Nonglycosylated Phenotype

phenotype

phenotype

Apolipoproteins E Measurement (Procedure)

phenotype

phenotype

Apoptotic Dna Damage

syndrome

disease

Apparent Mineralocorticoid Excess

syndrome

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

Apparent Mineralocorticoid Excess, Mild

phenotype

phenotype

Appendiceal Neoplasms

group

group · Digestive System Diseases; Neoplasms

Appendiceal Stump

phenotype

phenotype

Appendicitis

syndrome

ICD-10 K37

disease · Digestive System Diseases; Infections

Appendicolith

syndrome

disease

Appendicular Hypotonia

phenotype

phenotype · Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Appetite Disorders

group

group · Mental Disorders

Apraxia of Eyelid

phenotype

phenotype · Behavior and Behavior Mechanisms; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Apraxia of Phonation

syndrome

disease · Behavior and Behavior Mechanisms; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Apraxia, Articulatory

phenotype

phenotype · Behavior and Behavior Mechanisms; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Apraxia, Developmental Verbal

disease

disease · Behavior and Behavior Mechanisms; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Apraxia, Facial-Oral

phenotype

phenotype · Behavior and Behavior Mechanisms; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Apraxia, Gestural

phenotype

phenotype · Behavior and Behavior Mechanisms; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Apraxia, Ideomotor

disease

disease · Behavior and Behavior Mechanisms; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Apraxia, Motor

phenotype

phenotype · Behavior and Behavior Mechanisms; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Apraxia, Oculomotor, Cogan Type

disease

disease · Cardiovascular Diseases; Nervous System Diseases; Behavior and Behavior Mechanisms; Eye Diseases; Pathological Conditions, Signs and Symptoms

Apraxia, Oral

disease

disease · Behavior and Behavior Mechanisms; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Apraxia, Verbal

disease

disease · Behavior and Behavior Mechanisms; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Apraxias

group

ICD-10 R48.2

group · Behavior and Behavior Mechanisms; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Aprosencephaly

disease

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

Aprosodia

phenotype

phenotype · Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Aprt Deficiency, Japanese Type

syndrome

disease · Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases

Apudoma

disease

disease · Neoplasms

Aquagenic Pruritus

phenotype

phenotype · Skin and Connective Tissue Diseases; Immune System Diseases; Pathological Conditions, Signs and Symptoms

Aqueductal Stenosis

syndrome

disease · Nervous System Diseases