Condition

Absent Pigmentation of The Ventral Chest

syndrome

disease

Absent Pituitary

disease

disease

Absent Primary Metaphyseal Spongiosa

phenotype

phenotype

Absent Proximal Finger Flexion Creases

phenotype

phenotype

Absent Proximal Phalanx of Thumb

phenotype

phenotype

Absent Pubertal Growth Spurt

phenotype

phenotype

Absent Pubic Hair

phenotype

phenotype

Absent Radius

disease

disease

Absent Reflex

phenotype

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

Absent Retinal Pigment Epithelium

phenotype

phenotype

Absent Scaphoid

phenotype

phenotype

Absent Scrotum

disease

disease

Absent Skin Pigmentation

phenotype

phenotype · Skin and Connective Tissue Diseases

Absent Smooth Pursuit

phenotype

phenotype

Absent Specific Antibody Response

phenotype

phenotype

Absent Speech

phenotype

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

Absent Sperm Flagella

phenotype

phenotype

Absent Sternal Ossification

phenotype

phenotype

Absent Styloid Process of Ulna

disease

disease

Absent Testes

phenotype

phenotype

Absent Thumb, Bilateral

phenotype

phenotype

Absent Thumbnail

phenotype

phenotype

Absent Tibia

phenotype

phenotype

Absent Toe

disease

disease

Absent Toenail

phenotype

phenotype · Pathological Conditions, Signs and Symptoms

Absent Tragus

disease

disease

Absent Urinary Urothione

phenotype

phenotype

Absent Vertebral Body Mineralization

phenotype

phenotype

Absent Vestibular Function

phenotype

phenotype

Absent/Hypoplastic Coccyx

phenotype

phenotype

Absent/Hypoplastic Paranasal Sinuses

phenotype

phenotype

Absent/Shortened Outer Dynein Arms

phenotype

phenotype

Absssi

syndrome

disease

Abulia

disease

disease

Abuse Neglect

phenotype

phenotype

Abuse of Synthetic Cathinone

disease

disease · Mental Disorders; Chemically-Induced Disorders

Acalculous Cholecystitis

syndrome

disease · Digestive System Diseases

Acampomelic Campomelic Dysplasia

syndrome

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

Acanthamoeba Infection

syndrome

ICD-10 B60.1

disease · Infections

Acanthamoeba Keratitis

syndrome

disease · Eye Diseases; Infections

Acanthocheilonemiasis

syndrome

disease · Infections

Acanthocytosis

syndrome

disease · Hemic and Lymphatic Diseases

Acanthocytosis Due To Band 3 Ht

phenotype

phenotype

Acanthocytosis With Hypobetalipoproteinemia

syndrome

disease · Nutritional and Metabolic Diseases

Acantholysis

phenotype

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

Acantholytic Dyskeratotic Epidermal Nevus

disease

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

Acantholytic Squamous Cell Carcinoma

disease

disease · Neoplasms

Acanthoma

disease

disease · Neoplasms