Condition

Ataxia, Early-Onset, With Oculomotor Apraxia And Hypoalbuminemia

syndrome

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

Ataxia, Fatal X-Linked, With Deafness And Loss of Vision

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Eye Diseases; Pathological Conditions, Signs and Symptoms; Otorhinolaryngologic Diseases

Ataxia, Friedreich-Like, With Isolated Vitamin E Deficiency

disease

disease

Ataxia, Motor

phenotype

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

Ataxia, Progressive Seizures, Mental Deterioration, And Hearing Loss

disease

disease

Ataxia, Sensory

phenotype

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

Ataxia, Sensory, Autosomal Dominant

syndrome

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

Ataxia, Spastic, 1, Autosomal Dominant

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Ataxia, Spastic, 2, Autosomal Recessive (Disorder)

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Ataxia, Spastic, 3, Autosomal Recessive

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Ataxia, Spastic, Childhood-Onset, Autosomal Recessive, With Optic Atrophy And Mental Retardation

syndrome

disease

Ataxia, Spinocerebellar

syndrome

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

Ataxia, Truncal

phenotype

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

Ataxias, Hereditary

syndrome

ICD-10 G11.9; G11

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

Ataxic

phenotype

phenotype

Ataxic Cerebral Palsy

syndrome

ICD-10 G80.4

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Pathological Conditions, Signs and Symptoms

Atelectasis

phenotype

ICD-10 J98.1

phenotype · Respiratory Tract Diseases

Atelosteogenesis Type 2

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases

Atelosteogenesis Type 3

disease

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases

Atelosteogenesis, Type 1

disease

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases

Athabaskan Brainstem Dysgenesis

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Eye Diseases; Pathological Conditions, Signs and Symptoms; Otorhinolaryngologic Diseases

Athabaskan Severe Combined Immunodeficiency

syndrome

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

Atheroeruptive Xanthoma

syndrome

disease · Nutritional and Metabolic Diseases

Atherogenesis

phenotype

phenotype · Cardiovascular Diseases

Atherogenic Dyslipidaemia

syndrome

disease

Atheroma

phenotype

phenotype · Pathological Conditions, Signs and Symptoms

Atherosclerosis

syndrome

ICD-10 I25.0; I70

disease · Cardiovascular Diseases

Atherosclerosis Obliterans

syndrome

disease

Atherosclerosis of Aorta

phenotype

ICD-10 I70.0

phenotype · Cardiovascular Diseases

Atherosclerotic Lesion

syndrome

disease · Cardiovascular Diseases

Atherosclerotic Occlusive Disease

syndrome

disease · Cardiovascular Diseases

Atherosclerotic Parkinsonism

syndrome

disease · Nervous System Diseases

Atherosclerotic Renal Artery Stenosis

syndrome

disease · Cardiovascular Diseases; Male Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications

Atherothrombosis

disease

disease

Athetoid Cerebral Palsy

syndrome

ICD-10 G80.3

disease · Nervous System Diseases

Athetosis

phenotype

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

Athlete'S Heart

syndrome

disease · Cardiovascular Diseases; Pathological Conditions, Signs and Symptoms

Atkin Syndrome

syndrome

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

Atlantoaxial Abnormality

phenotype

phenotype

Atlantoaxial Instability

syndrome

disease

Atonic Absence Seizures

phenotype

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

Atopic Asthma, Susceptibility To

phenotype

phenotype

Atopic Cataract

syndrome

disease · Eye Diseases

Atopic Dermatitis

disease

Atopic Disorders

group

group

Atopic Eczema/Dermatitis (Non-Specific)

syndrome

disease · Immune System Diseases; Skin and Connective Tissue Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Atopic Ige-Mediated Allergic Disorder

syndrome

disease · Immune System Diseases

Atopic Keratoconjunctivitis

syndrome

disease · Eye Diseases; Immune System Diseases