# group[].element[].display
Delay when starting to pass urine (finding)

# group[].element[].display
Congenital anomaly of pharynx (disorder)

# group[].element[].display
Abnormal nervous system function (finding)

# group[].element[].display
Congenital anomaly of urethra (disorder)

# group[].element[].display
Congenital anomaly of middle ear (disorder)

# group[].element[].display
Congenital anomaly of the peripheral nervous system (disorder)

# group[].element[].target[].display
Abnormal peripheral nervous system morphology

# group[].element[].display
Congenital anomaly of the thyroid gland (disorder)

# group[].element[].display
Congenital hypoplasia of kidney (disorder)

# group[].element[].target[].display
Abnormalities of placenta or umbilical cord

# group[].element[].display
Congenital anomaly of the hand (disorder)

# group[].element[].display
Congenital hypoplasia of penis (disorder)

# group[].element[].display
Paresis of extraocular muscles (disorder)

# group[].element[].display
Congenital anomaly of the bladder (disorder)

# group[].element[].display
Congenital anomaly of the bladder (disorder)

# group[].element[].display
Congenital anomaly of the thymus (disorder)

# group[].element[].display
Urinary incontinence of non-organic origin (finding)

# group[].element[].display
Submucous cleft of hard palate (disorder)

# group[].element[].display
Congenital anomaly of the kidney (disorder)

# group[].element[].display
Disorder of skin pigmentation (disorder)

# group[].element[].display
Congenital dislocation of hip (disorder)

# group[].element[].display
Congenital anomaly of adrenal gland (disorder)

# group[].element[].display
Delayed articulatory and language development (finding)

# group[].element[].display
Partial congenital absence of teeth (disorder)

# group[].element[].display
Partial congenital absence of teeth (disorder)

# group[].element[].display
Congenital anomaly of parathyroid glands (disorder)

# group[].element[].display
Congenital anomaly of upper limb (disorder)

# group[].element[].display
Congenital atresia of external auditory canal (disorder)

# group[].element[].display
Mixed conductive AND sensorineural hearing loss (disorder)

# group[].element[].display
Congenital elevation of scapula (disorder)

# group[].element[].display
Congenital cystic kidney disease (disorder)

# group[].element[].display
Congenital anomaly of diaphragm (disorder)

# group[].element[].display
Congenital abnormal fusion of metatarsal bone (disorder)

# group[].element[].display
Congenital abnormal shape of clavicle (disorder)

# group[].element[].display
Congenital abnormal shape of pinna (disorder)

# group[].element[].display
Congenital hypoplasia of adrenal gland (disorder)

# group[].element[].display
Congenital hypoplasia of carpal bone (disorder)

# group[].element[].display
Congenital hypoplasia of thymus (disorder)

# group[].element[].display
Hypoplasia of the optic nerve (disorder)

# group[].element[].display
Abnormal visual evoked potential (finding)

# group[].element[].display
Blindness AND/OR vision impairment level (disorder)

# group[].element[].display
Congenital anomaly of scapula (disorder)

# group[].element[].display
Congenital anomaly of carpal bone (disorder)

# group[].element[].display
Congenital anomaly of metacarpal bone (disorder)

# group[].element[].display
Congenital anomaly of maxilla (disorder)

# group[].element[].display
Increased human growth hormone level (finding)

# group[].element[].display
On examination - external female genitalia abnormal (finding)

# group[].element[].target[].display
Abnormality of female external genitalia

# group[].element[].display
Smooth pursuit movement deficiency (finding)

# group[].element[].display
Recurrent urinary tract infection (disorder)

# group[].element[].display
Congenital malformation of corpus callosum (disorder)

# group[].element[].display
Stenosis of nasolacrimal duct (disorder)

# group[].element[].display
Congenital abnormality of scrotum (disorder)

# group[].element[].display
Abnormal saccadic eye movement (disorder)

# group[].element[].display
Upward slant of palpebral fissure (finding)

# group[].element[].display
Downward slant of palpebral fissure (finding)

# group[].element[].display
Shallow anterior chamber of eye (finding)

# group[].element[].display
Single transverse palmar crease (finding)

# group[].element[].display
Partial agenesis of corpus callosum (disorder)

# group[].element[].display
Congenital malformation of the eyebrow (disorder)

# group[].element[].display
Congenital anterior polar cataract (disorder)

# group[].element[].display
Congenital posterior polar cataract (disorder)

# group[].element[].display
Congenital malformation of the urinary system (disorder)

# group[].element[].display
Congenital malformation of sternum (disorder)

# group[].element[].display
Autosomal dominant inheritance (qualifier value)

# group[].element[].display
Small for gestational age fetus (disorder)

# group[].element[].display
Congenital abnormality of liver and/or biliary tract (disorder)

# group[].element[].display
Dementia of frontal lobe type (disorder)

# group[].element[].display
Congenital abnormality of oral cavity (disorder)

# group[].element[].display
Range of joint movement increased (finding)

# group[].element[].display
Stenosis of external auditory canal (disorder)

# group[].element[].display
Opening of lower lacrimal punctum absent (finding)

# group[].element[].display
Congenital anomaly of abdomen (disorder)

# group[].element[].display
Finding of range of thumb abduction (finding)

# group[].element[].display
Finding of range of thumb adduction (finding)

# group[].element[].display
Narrowing of palpebral fissure (finding)

# group[].element[].display
Congenital malformation of thumb (disorder)

# group[].element[].target[].display
Congenital fibrosis of extraocular muscles

# group[].element[].display
Degenerative disorder of macula (disorder)

# group[].element[].display
Short vertical length of upper lip (finding)

# group[].element[].display
Localized hypoplasia of tooth (disorder)

# group[].element[].display
Congenital duplication of renal collecting system (disorder)

# group[].element[].display
Congenital coloboma of macula lutea (disorder)

# group[].element[].display
Isolated hypoplasia of cerebellar vermis (disorder)

# group[].element[].display
Anterior pituitary hormone deficiency (disorder)

# group[].element[].display
Dermoid choristoma of eye proper (disorder)

# group[].element[].display
Congenital transverse septate vagina (disorder)

# group[].element[].display
Late closure of anterior fontanel (finding)

# group[].element[].target[].display
Delayed closure of the anterior fontanelle

# group[].element[].display
Large for gestational age newborn (finding)

# group[].element[].display
Double outlet right ventricle (disorder)

# group[].element[].display
Disorder of hematopoietic structure (disorder)

# group[].element[].target[].display
Abnormality of blood and blood-forming tissues

# group[].element[].display
Congenital malformation of the respiratory system (disorder)

# group[].element[].display
Profound mental retardation (Intelligence Quotient below 20) (disorder)

# group[].element[].display
Gross motor development delay (disorder)

# group[].element[].display
Moderate mental retardation (Intelligence Quotient 35-49) (disorder)

# group[].element[].display
Simple partial seizure, consciousness not impaired (disorder)

# group[].element[].target[].display
Focal seizures without impairment of consciousness or awareness

# group[].element[].display
Partial seizure with impaired consciousness (disorder)

# group[].element[].target[].display
Focal seizures with impairment of consciousness or awareness

# group[].element[].display
Cleft palate and bilateral cleft lip (disorder)

# group[].element[].display
Obstructive sleep apnea syndrome (disorder)

# group[].element[].display
Disorder of skeletal AND/OR smooth muscle (disorder)

# group[].element[].display
Increased creatine kinase level (finding)

# group[].element[].display
Flexion contracture of toe joint (disorder)

# group[].element[].display
Flexion contracture of the knee (disorder)

# group[].element[].display
Ligamentous laxity of ankle region (disorder)

# group[].element[].display
Abnormal auditory evoked potential (finding)

# group[].element[].display
Congenital sensorineural hearing loss (disorder)

# group[].element[].display
Severe mental retardation (Intelligence Quotient 20-34) (disorder)

# group[].element[].display
Congenital anomaly of gastrointestinal tract (disorder)

# group[].element[].target[].display
Abnormality of the gastrointestinal tract

# group[].element[].display
Eyelid myoclonus with absences (disorder)

# group[].element[].display
Multiple muscular ventricular septum defect (disorder)

# group[].element[].target[].display
Multiple muscular ventricular septal defects

# group[].element[].display
Inflammatory disease of liver (disorder)

# group[].element[].display
Developmental delay in social skills (disorder)