Condition

Autosomal Dominant Oculocutaneous Albinism

disease

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

Autosomal Dominant Optic Atrophy Plus Syndrome

syndrome

disease · Cardiovascular Diseases; Nervous System Diseases; Nutritional and Metabolic Diseases; Eye Diseases; Pathological Conditions, Signs and Symptoms; Musculoskeletal Diseases

Autosomal Dominant Osteopetrosis

syndrome

disease · Musculoskeletal Diseases

Autosomal Dominant Parkinsonism

syndrome

disease · Nervous System Diseases

Autosomal Dominant Primary Hypomagnesemia With Hypocalciuria

phenotype

phenotype · Female Urogenital Diseases and Pregnancy Complications; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Male Urogenital Diseases; Pathological Conditions, Signs and Symptoms

Autosomal Dominant Retinitis Pigmentosa

disease

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

Autosomal Dominant Spondylocostal Dysostosis

syndrome

disease · Musculoskeletal Diseases

Autosomal Dominant Tubulointerstitial Kidney Disease

syndrome

disease

Autosomal Dominant Vitreoretinochoroidopathy

syndrome

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

Autosomal Hemophilia A

syndrome

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

Autosomal Recessive Agammaglobulinemia

syndrome

disease

Autosomal Recessive Centronuclear Myopathy

syndrome

disease · Nervous System Diseases; Musculoskeletal Diseases

Autosomal Recessive Cerebellar Ataxia Type 1

syndrome

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

Autosomal Recessive Cerebellar Ataxia With Late-Onset Spasticity

syndrome

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

Autosomal Recessive Cerebellar Ataxia With Oculomotor Apraxia Type 1

syndrome

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

Autosomal Recessive Cerebellar Ataxia, Epilepsy, Intellectual Disability Syndrome Due To Wwox Deficiency

syndrome

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

Autosomal Recessive Cerebral Atrophy

syndrome

disease

Autosomal Recessive Chronic Granulomatous Disease

syndrome

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

Autosomal Recessive Congenital Methemoglobinemia Type I

syndrome

disease · Hemic and Lymphatic Diseases

Autosomal Recessive Cutis Laxa Type 2B

syndrome

disease · Nutritional and Metabolic Diseases; Musculoskeletal Diseases

Autosomal Recessive Emery-Dreifuss Muscular Dystrophy

syndrome

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

Autosomal Recessive Facio-Digito-Genital Syndrome

syndrome

disease · Endocrine System Diseases; Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases

Autosomal Recessive Familial Dystonia

syndrome

disease · Nervous System Diseases

Autosomal Recessive Hereditary Spastic Paraplegia

syndrome

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

Autosomal Recessive Hyperimmunoglobulin M Syndrome

syndrome

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

Autosomal Recessive Hypophosphatemic Vitamin D Refractory Rickets

syndrome

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

Autosomal Recessive Ichthyosis

disease

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

Autosomal Recessive Limb Girdle Muscular Dystrophy Type 2A

syndrome

disease

Autosomal Recessive Limb Girdle Muscular Dystrophy Type 2B

syndrome

disease

Autosomal Recessive Limb Girdle Muscular Dystrophy Type 2D

syndrome

disease

Autosomal Recessive Limb Girdle Muscular Dystrophy Type 2S

syndrome

disease

Autosomal Recessive Lower Motor Neuron Disease With Childhood Onset

syndrome

disease · Nervous System Diseases

Autosomal Recessive Myogenic Arthrogryposis Multiplex Congenita

syndrome

disease

Autosomal Recessive Ocular Albinism

disease

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

Autosomal Recessive Osteopetrosis

syndrome

disease · Musculoskeletal Diseases

Autosomal Recessive Parkinsonism

syndrome

disease · Nervous System Diseases

Autosomal Recessive Polycystic Kidney Disease

syndrome

ICD-10 Q61.1

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

Autosomal Recessive Primary Microcephaly

syndrome

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

Autosomal Recessive Retinitis Pigmentosa

disease

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

Autosomal Recessive Scid

syndrome

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

Autosomal Recessive Sideroblastic Anemia

syndrome

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

Autosomal Recessive Spastic Paraplegia Type 59

syndrome

disease

Autosomal Recessive Spastic Paraplegia Type 67

syndrome

disease

Autosomal Recessive Spastic Paraplegia Type 70

syndrome

disease

Autosomal Systemic Lupus Erythematosus

syndrome

disease · Skin and Connective Tissue Diseases; Immune System Diseases

Autosome Abnormalities

group

group · Pathological Conditions, Signs and Symptoms

Autotomy

disease

disease

Av Block First Degree By Ecg Finding

phenotype

phenotype · Cardiovascular Diseases; Pathological Conditions, Signs and Symptoms