Condition

46,Xx Sex Reversal 3

syndrome

disease

46,Xx Sex Reversal 4

disease

disease

46,Xy Disorder of Sex Development Due To Lh Defects

syndrome

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

46,Xy Gonadal Dysgenesis, Complete Or Partial, Dhh-Related

disease

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

46,Xy Gonadal Dysgenesis, Complete, Sry-Related

syndrome

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

46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy

syndrome

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

46,Xy Partial Gonadal Dysgenesis

syndrome

disease

46,Xy Sex Reversal 3

disease

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

46,Xy Sex Reversal 4

disease

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

46,Xy Sex Reversal 6

syndrome

disease

46,Xy Sex Reversal 9

syndrome

disease

46,Xy True Hermaphroditism, Sry-Related

syndrome

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

47, Xyy Syndrome

syndrome

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

4P16.3 Microduplication Syndrome

syndrome

disease

4Q Partial Monosomy Syndrome

syndrome

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

4Q21 Microdeletion Syndrome

phenotype

phenotype · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Pathological Conditions, Signs and Symptoms

5-Alpha Reductase Deficiency

syndrome

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

5-Minute Apgar Score of 1

phenotype

phenotype

5-Minute Apgar Score of 5

phenotype

phenotype

5-Oxoprolinase Deficiency

syndrome

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

5,10-Methylenetetrahydrofolate Reductase Deficiency

syndrome

disease · Nutritional and Metabolic Diseases

5P13 Microduplication Syndrome

syndrome

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

5Q-Syndrome

syndrome

disease · Hemic and Lymphatic Diseases; Pathological Conditions, Signs and Symptoms

5Q14.3 Microdeletion Syndrome

syndrome

disease

5Q35 Microduplication Syndrome

syndrome

disease

6 Alpha Mercaptopurine Sensitivity

syndrome

disease · Immune System Diseases; Chemically-Induced Disorders; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases

6 Metacarpals

phenotype

phenotype

6-Phosphogluconolactonase Deficiency

syndrome

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

6-Pyruvoyl-Tetrahydropterin Synthase Deficiency

syndrome

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

6Q Terminal Deletion Syndrome

syndrome

disease

6Q24-Related Transient Neonatal Diabetes Mellitus

syndrome

disease · Nutritional and Metabolic Diseases; Endocrine System Diseases

6Q25 Microdeletion Syndrome

syndrome

disease

7-Dehydrocholesterol Reductase Deficiency

syndrome

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

7Q31 Microdeletion Syndrome

syndrome

disease

8P11.2 Deletion Syndrome

syndrome

disease

9P Partial Monosomy Syndrome

syndrome

disease · Pathological Conditions, Signs and Symptoms

9Q22.3 Microdeletion

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Aa Amyloidosis

syndrome

disease · Nutritional and Metabolic Diseases

Aarskog Syndrome

syndrome

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

Aase Smith Syndrome 2

syndrome

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

Aase Syndrome

syndrome

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

Abcd Syndrome

syndrome

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Abdomen Distended

phenotype

phenotype · Digestive System Diseases

Abdomen, Acute

phenotype

ICD-10 R10.0

phenotype · Pathological Conditions, Signs and Symptoms

Abdominal Abscess

syndrome

disease · Infections

Abdominal Adhesions

disease

disease · Digestive System Diseases

Abdominal aortic aneurysm

disease

Abdominal Aortic Atherosclerosis

syndrome

disease