Condition

Aphasia, Post-Ictal

phenotype

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

Aphasia, Post-Traumatic

phenotype

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

Aphasia, Progressive

disease

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

Aphasia, Semantic

phenotype

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

Aphasia, Syntactical

phenotype

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

Aphasic

phenotype

phenotype

Aphonia

phenotype

ICD-10 R49.1

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

Aphthous Stomatitis

syndrome

disease · Stomatognathic Diseases

Apical Hypertrophic Cardiomyopathy

syndrome

disease · Cardiovascular Diseases

Apical Myocardial Infarction

syndrome

disease

Aplasia Cutis Congenita

disease

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

Aplasia Cutis Congenita of Scalp

disease

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

Aplasia Cutis Congenita On Trunk Or Limbs

phenotype

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

Aplasia Cutis Congenita Over Posterior Parietal Area

disease

disease

Aplasia Cutis Congenita Over The Scalp Vertex

disease

disease

Aplasia Cutis Congenita With Epibulbar Dermoids

syndrome

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

Aplasia of Lacrimal And Salivary Glands

disease

disease · Eye Diseases; Stomatognathic Diseases

Aplasia of Metacarpal Bones

phenotype

phenotype

Aplasia of Muscle

disease

disease · Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Aplasia of Optic Nerve

phenotype

phenotype

Aplasia of The 1St Metacarpal

phenotype

phenotype

Aplasia of The 2Nd Metacarpal

phenotype

phenotype

Aplasia of The 4Th Metacarpal

phenotype

phenotype

Aplasia of The Abdominal Wall Musculature

phenotype

phenotype

Aplasia of The Bladder

phenotype

phenotype

Aplasia of The Distal Phalanges of The Hand

phenotype

phenotype

Aplasia of The Distal Phalanx of The Hallux

phenotype

phenotype

Aplasia of The Epiglottis

disease

disease

Aplasia of The Inferior Half of The Cerebellar Vermis

phenotype

phenotype

Aplasia of The Maxilla

phenotype

phenotype

Aplasia of The Middle Phalanges of The Toes

phenotype

phenotype

Aplasia of The Middle Phalanx of The Hand

phenotype

phenotype

Aplasia of The Parotid Gland

disease

disease

Aplasia of The Pectoralis Major Muscle

disease

disease

Aplasia of The Phalanges of The 3Rd Toe

phenotype

phenotype

Aplasia of The Phalanges of The Hand

phenotype

phenotype

Aplasia of The Proximal Phalanges of The Hand

phenotype

phenotype

Aplasia of The Semicircular Canal

disease

disease

Aplasia of The Sweat Glands

phenotype

phenotype

Aplasia of The Tarsal Bones

phenotype

phenotype

Aplasia of The Ulna

phenotype

phenotype

Aplasia of The Vagina

phenotype

phenotype

Aplasia/Hypoplasia Affecting The Eye

phenotype

phenotype

Aplasia/Hypoplasia Involving The Carpal Bones

phenotype

phenotype

Aplasia/Hypoplasia Involving The Central Nervous System

phenotype

phenotype

Aplasia/Hypoplasia Involving The Metacarpal Bones

phenotype

phenotype

Aplasia/Hypoplasia Involving The Nose

phenotype

phenotype

Aplasia/Hypoplasia Involving The Pelvis

phenotype

phenotype