Condition

Alzheimer Disease, Familial, 3, With Spastic Paraparesis And Unusual Plaques

syndrome

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

Alzheimer Disease, Familial, 3, With Unusual Plaques

disease

disease

Alzheimer Disease, Familial, Type 3

syndrome

disease · Mental Disorders; Nervous System Diseases

Alzheimer Disease, Familial, With Spastic Paraparesis And Unusual Plaques

disease

disease

Alzheimer Disease, Late Onset

disease

ICD-10 F00.1; G30.1

disease · Mental Disorders; Nervous System Diseases

Alzheimer Disease, Susceptibility To

phenotype

phenotype

Alzheimer Disease, Susceptibility To, Mitochondrial

disease

disease

Alzheimer'S Disease

syndrome

ICD-10 G30.9; G30

disease · Mental Disorders; Nervous System Diseases

Alzheimer'S Disease, Focal Onset

disease

disease · Mental Disorders; Nervous System Diseases

Amaurosis

syndrome

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

Amaurosis Congenita of Leber, Type 1

syndrome

disease · Eye Diseases

Amaurosis Fugax

phenotype

ICD-10 G45.3

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

Amaurosis Hypertrichosis

syndrome

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

Amaurotic Familial Idiocy

syndrome

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

Ambiguous Genitalia

disease

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

Ambiguous Genitalia, Female

disease

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

Ambiguous Genitalia, Male

phenotype

phenotype · Male Urogenital Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases

Amblyopia

phenotype

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

Amebiasis

syndrome

ICD-10 A06.9; A06

disease · Infections

Amebic Colitis

syndrome

disease · Digestive System Diseases; Infections

Amegakaryocytic Thrombocytopenia

syndrome

disease · Hemic and Lymphatic Diseases

Amegakaryocytosis

syndrome

disease

Amelanotic Skin Melanoma

disease

disease · Skin and Connective Tissue Diseases; Neoplasms

Amelia

disease

ICD-10 Q73.0

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

Amelia Involving The Lower Limbs

disease

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

Ameloblastic Carcinoma

disease

disease

Ameloblastic Fibroma

disease

disease · Neoplasms

Ameloblastoma

disease

disease · Neoplasms

Amelogenesis Imperfecta

disease

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

Amelogenesis Imperfecta And Gingival Hyperplasia Syndrome

disease

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

Amelogenesis Imperfecta Hypomaturation Type

disease

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

Amelogenesis Imperfecta Local Hypoplastic Form

disease

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

Amelogenesis Imperfecta Nephrocalcinosis

syndrome

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

Amelogenesis Imperfecta Pigmented Hypomaturation Type

disease

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

Amelogenesis Imperfecta, Hypocalcified Type (Primary And Secondary Teeth)

phenotype

phenotype

Amelogenesis Imperfecta, Hypomaturation Hypoplasia Type With Taurodontism

disease

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

Amelogenesis Imperfecta, Hypomaturation Type, Iia1

syndrome

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

Amelogenesis Imperfecta, Hypomaturation Type, Iia2

syndrome

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

Amelogenesis Imperfecta, Hypomaturation Type, Iia3

syndrome

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

Amelogenesis Imperfecta, Hypomaturation Type, Iia4

syndrome

disease

Amelogenesis Imperfecta, Hypomaturation Type, Iia5

syndrome

disease

Amelogenesis Imperfecta, Hypomaturation Type, Iia6

syndrome

disease

Amelogenesis Imperfecta, Hypomaturation Type, With Snow-Capped Teeth

syndrome

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

Amelogenesis Imperfecta, Hypoplastic/Hypomaturation, X-Linked 1

syndrome

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

Amelogenesis Imperfecta, Type Ia

syndrome

disease

Amelogenesis Imperfecta, Type Ib

syndrome

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

Amelogenesis Imperfecta, Type Ic

syndrome

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

Amelogenesis Imperfecta, Type If

syndrome

disease