Condition

Abnormal Palmar Creases

disease

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

Abnormal Palmar Dermatoglyphics

disease

disease

Abnormal Pancreatic Duct Morphology

phenotype

phenotype

Abnormal Parietal Bone Morphology

phenotype

phenotype

Abnormal Parotid Gland Morphology

phenotype

phenotype

Abnormal Pattern of Respiration

phenotype

phenotype

Abnormal Pelvis Bone Morphology

phenotype

phenotype

Abnormal Pelvis Bone Ossification

disease

disease

Abnormal Pericardium Morphology

phenotype

phenotype · Cardiovascular Diseases; Congenital, Hereditary, and Neonatal Diseases and Abnormalities

Abnormal Perifollicular Morphology

phenotype

phenotype

Abnormal Peripheral Myelination

disease

disease

Abnormal Peripheral Nervous System Morphology

disease

disease

Abnormal Peristalsis

phenotype

phenotype

Abnormal Pigmentation

phenotype

phenotype

Abnormal Pigmentation of The Oral Mucosa

phenotype

phenotype

Abnormal Platelet Function

phenotype

phenotype

Abnormal Platelet Granules

disease

disease

Abnormal Platelet Morphology

phenotype

phenotype

Abnormal Platelet Shape

disease

disease

Abnormal Platelets

phenotype

phenotype · Hemic and Lymphatic Diseases

Abnormal Position of Hair Whorl

phenotype

phenotype

Abnormal Posture

phenotype

ICD-10 R29.3

phenotype · Nervous System Diseases

Abnormal Proerythroblast Morphology

phenotype

phenotype

Abnormal Prolactin Level

phenotype

phenotype

Abnormal Proportion of Cd4 T Cells

phenotype

phenotype

Abnormal Proportion of Cd8 T Cells

phenotype

phenotype

Abnormal Protein N-Linked Glycosylation

phenotype

phenotype

Abnormal Protein O-Linked Glycosylation

phenotype

phenotype

Abnormal Pulmonary Valve Cusp Morphology

phenotype

phenotype

Abnormal Pulmonary Vein Morphology

phenotype

phenotype

Abnormal Pupillary Light Reflex

phenotype

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

Abnormal Putamen Morphology

phenotype

phenotype

Abnormal Rapid Eye Movement Sleep

phenotype

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

Abnormal Renal Corticomedullary Differentiation

phenotype

phenotype

Abnormal Renal Function

phenotype

phenotype · Male Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications

Abnormal Renal Morphology

disease

ICD-10 Q63.9

disease

Abnormal Reproductive System Morphology

phenotype

phenotype

Abnormal Respiratory Motile Cilium Morphology

disease

disease

Abnormal Respiratory System Morphology

phenotype

phenotype

Abnormal Response To Acth Stimulation Test

phenotype

phenotype

Abnormal Retinal Morphology

phenotype

phenotype · Eye Diseases

Abnormal Saccadic Eye Movement

disease

disease

Abnormal Sacral Segmentation

phenotype

phenotype

Abnormal Sacrum Morphology

disease

disease

Abnormal Salivary Gland Morphology

phenotype

phenotype · Stomatognathic Diseases

Abnormal Sclera Morphology

phenotype

phenotype

Abnormal Scrotal Rugation

disease

disease

Abnormal Sensory Nerve Conduction Velocity

phenotype

phenotype