Condition

Abnormality of Masticatory Muscle

phenotype

phenotype

Abnormality of Mesentery Morphology

phenotype

phenotype

Abnormality of Metabolism/Homeostasis

phenotype

phenotype

Abnormality of Midbrain Morphology

phenotype

phenotype

Abnormality of Mitochondrial Metabolism

phenotype

phenotype

Abnormality of Mouth Size

phenotype

phenotype

Abnormality of Mucopolysaccharide Metabolism

phenotype

phenotype

Abnormality of Multiple Cell Lineages In The Bone Marrow

disease

disease

Abnormality of Muscle Fibers

phenotype

phenotype

Abnormality of Muscle Size

phenotype

phenotype

Abnormality of Nail Color

disease

disease · Pathological Conditions, Signs and Symptoms

Abnormality of Nail of Toe

phenotype

phenotype · Pathological Conditions, Signs and Symptoms

Abnormality of Nasopharyngeal Adenoids

phenotype

phenotype

Abnormality of Neck Blood Vessel

disease

disease

Abnormality of Nervous System Morphology

disease

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

Abnormality of Nervous System Physiology

phenotype

phenotype · Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases

Abnormality of Neurogenesis

disease

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

Abnormality of Neutrophil Morphology

phenotype

phenotype

Abnormality of Neutrophil Physiology

phenotype

phenotype

Abnormality of Ocular Abduction

phenotype

phenotype

Abnormality of Ocular Smooth Pursuit

phenotype

phenotype

Abnormality of Ornithine Metabolism

phenotype

phenotype

Abnormality of Pain Sensation

phenotype

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

Abnormality of Pelvic Girdle Bone Morphology

disease

disease

Abnormality of Peripheral Nerve Conduction

phenotype

phenotype

Abnormality of Placental Membranes

phenotype

phenotype

Abnormality of Prenatal Development Or Birth

disease

disease

Abnormality of Primary Molar Morphology

disease

disease

Abnormality of Primary Teeth

phenotype

phenotype

Abnormality of Pulmonary Valve

disease

disease

Abnormality of Radial Ray

phenotype

phenotype

Abnormality of Red Blood Cells

group

ICD-10 R71

group · Hemic and Lymphatic Diseases

Abnormality of Refraction

disease

disease

Abnormality of Renal Excretion

disease

disease

Abnormality of Reproductive System Physiology

phenotype

phenotype

Abnormality of Retinal Pigmentation

phenotype

phenotype

Abnormality of Salivation

phenotype

phenotype

Abnormality of Secondary Sexual Hair

disease

disease

Abnormality of Skeletal Maturation

phenotype

phenotype

Abnormality of Skeletal Morphology

phenotype

phenotype

Abnormality of Skeletal Muscle Fiber Size

phenotype

phenotype

Abnormality of Skin Adnexa Morphology

phenotype

phenotype

Abnormality of Skin Morphology

phenotype

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

Abnormality of Skull Size

phenotype

phenotype

Abnormality of Somatosensory Evoked Potentials

phenotype

phenotype

Abnormality of Subcutaneous Fat Tissue

phenotype

phenotype

Abnormality of T Cell Physiology

phenotype

phenotype

Abnormality of T Cells

phenotype

phenotype