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NDD_ICD10_CODES:
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      - F80.9 Development disorder of speech & language, unspecified
      - F84.9 Pervasive developmental disorder, unspecified
      - R62.0 Delayed milestone in childhood
      - Z13.40 Encounter for screening for unspecified developmental delays
      - F82 Specific developmental disorder of motor function
      - F84.0 Autistic disorder
      - Q75.3 Macrocephaly
      - F70 Mild intellectual disability
      - F71 Moderate intellectual disability
      - F72 Severe intellectual disability
      - F73 Profound intellectual disability
      - Q89.9 Congenital malformation, unspecified
      - F88.0 Other disorders of psychological development (GDD)
      - G40.001 Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, with status epilepticus
      - G40.009 Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, not intractable, without status epilepticus
      - G40.011 Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, with status epilepticus
      - G40.019 Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localized onset, intractable, without status epilepticus
      - G40.101 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, with status epilepticus
      - G40.109 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, not intractable, without status epilepticus
      - G40.111 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, with status epilepticus
      - G40.119 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures, intractable, without status epilepticus
      - G40.201 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, with status epilepticus
      - G40.209 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, not intractable, without status epilepticus
      - G40.211 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, with status epilepticus
      - G40.219 Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures, intractable, without status epilepticus
      - G40.301 Generalized idiopathic epilepsy and epileptic syndromes, not intractable, with status epilepticus
      - G40.309 Generalized idiopathic epilepsy and epileptic syndromes, not intractable, without status epilepticus
      - G40.311 Generalized idiopathic epilepsy and epileptic syndromes, intractable, with status epilepticus
      - G40.319 Generalized idiopathic epilepsy and epileptic syndromes, intractable, without status epilepticus
      - G40.401 Other generalized epilepsy and epileptic syndromes, not intractable, with status epilepticus
      - G40.409 Other generalized epilepsy and epileptic syndromes, not intractable, without status epilepticus
      - G40.411 Other generalized epilepsy and epileptic syndromes, intractable, with status epilepticus
      - G40.419 Other generalized epilepsy and epileptic syndromes, intractable, without status epilepticus
      - G40.42 Cyclin-Dependent Kinase-Like 5 Deficiency Disorder
      - G40.501 Epileptic seizures related to external causes, not intractable, with status epilepticus
      - G40.509 Epileptic seizures related to external causes, not intractable, without status epilepticus
      - G40.801 Other epilepsy, not intractable, with status epilepticus
      - G40.802 Other epilepsy, not intractable, without status epilepticus
      - G40.803 Other epilepsy, intractable, with status epilepticus
      - G40.804 Other epilepsy, intractable, without status epilepticus
      - G40.811 Lennox-Gastaut syndrome, not intractable, with status epilepticus
      - G40.812 Lennox-Gastaut syndrome, not intractable, without status epilepticus
      - G40.813 Lennox-Gastaut syndrome, intractable, with status epilepticus
      - G40.814 Lennox-Gastaut syndrome, intractable, without status epilepticus
      - G40.821 Epileptic spasms, not intractable, with status epilepticus
      - G40.822 Epileptic spasms, not intractable, without status epilepticus
      - G40.823 Epileptic spasms, intractable, with status epilepticus
      - G40.824 Epileptic spasms, intractable, without status epilepticus
      - G40.833 Dravet syndrome, intractable, with status epilepticus
      - G40.834 Dravet syndrome, intractable, without status epilepticus
      - G40.841 KCNQ2-related epilepsy, not intractable, with status epilepticus
      - G40.842 KCNQ2-related epilepsy, not intractable, without status epilepticus
      - G40.843 KCNQ2-related epilepsy, intractable, with status epilepticus
      - G40.844 KCNQ2-related epilepsy, intractable, without status epilepticus
      - G40.89 Other seizures
      - G40.901 Epilepsy, unspecified, not intractable, with status epilepticus
      - G40.909 Epilepsy, unspecified, not intractable, without status epilepticus
      - G40.911 Epilepsy, unspecified, intractable, with status epilepticus
      - G40.919 Epilepsy, unspecified, intractable, without status epilepticus
      - G40.A01 Absence epileptic syndrome, not intractable, with status epilepticus
      - G40.A09 Absence epileptic syndrome, not intractable, without status epilepticus
      - G40.A11 Absence epileptic syndrome, intractable, with status epilepticus
      - G40.A19 Absence epileptic syndrome, intractable, without status epilepticus
      - G40.B01 Juvenile myoclonic epilepsy, not intractable, with status epilepticus
      - G40.B09 Juvenile myoclonic epilepsy, not intractable, without status epilepticus
      - G40.B11 Juvenile myoclonic epilepsy, intractable, with status epilepticus
      - G40.B19 Juvenile myoclonic epilepsy, intractable, without status epilepticus
      - G40.C01 Lafora progressive myoclonus epilepsy, not intractable, with status epilepticus
      - G40.C09 Lafora progressive myoclonus epilepsy, not intractable, without status epilepticus
      - G40.C11 Lafora progressive myoclonus epilepsy, intractable, with status epilepticus
      - G40.C19 Lafora progressive myoclonus epilepsy, intractable, without status epilepticus
      - P92.01 Bilious vomiting of newborn
      - P92.09 Other vomiting of newborn
      - P92.1 Regurgitation and rumination of newborn
      - P92.2 Slow feeding of newborn
      - P92.3 Underfeeding of newborn
      - P92.4 Overfeeding of newborn
      - P92.5 Neonatal difficulty in feeding at breast
      - P92.6 Failure to thrive in newborn
      - P92.8 Other feeding problems of newborn
      - P92.9 Feeding problem of newborn, unspecified
      - Z81.0 Family history of intellectual disabilities
      - Z81.1 Family history of alcohol abuse and dependence
      - Z81.2 Family history of tobacco abuse and dependence
      - Z81.3 Family history of other psychoactive substance abuse and dependence
      - Z81.4 Family history of other substance abuse and dependence
      - Z81.8 Family history of other mental and behavioral disorders
      - Z82.0 Family history of epilepsy and other diseases of the nervous system
      - Z82.79 Family history of other congenital malformations, deformations and chromosomal abnormalities
      - Z84.81 Family history of carrier of genetic disease
      - Z84.82 Family history of sudden infant death syndrome
CLINICAL_PHENOTYPES__DEVELOPMENTAL_BEHAVIORAL:
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    choices:
      - Attention deficit hyperactivity disorder
      - Anxiety
      - Autism
      - Austistic behavior
      - Behavioral abnormality
      - Bipolar affective disorder
      - Delayed motor development
      - Delayed speech & language development
      - Depressivity
      - Intellectual disability
      - Oppositional defiant disorder
      - Specific learning disability
    additionalInfoNeeded:
      - Behavioral abnormality
CLINICAL_PHENOTYPES__PERINATAL_HISTORY:
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    choices:
      - Abnormality of prenatal development or birth
      - Intrauterine growth restriction (IUGR)
      - Oligohydramnios
      - Polyhydramnios
      - Premature birth
    additionalInfoNeeded:
      - Abnormality of prenatal development or birth
CLINICAL_PHENOTYPES__CRANIOFACIAL:
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    choices:
      - Abnormal facial shape
      - Abnormality of the head
      - Abnormality of the pinna (ear malformation)
      - Cataract
      - Cleft lip
      - Cleft palate
      - Coloboma
      - Craniosynostosis
      - Hearing impairment
      - Macrocephaly
      - Microcephaly
    additionalInfoNeeded:
      - Abnormality of the head
CLINICAL_PHENOTYPES__CARDIAC:
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    choices:
      - Aortic root aneurysm
      - Arrhythmia
      - Atrial septal defect
      - Atrioventricular canal defect
      - Cardiomyopathy
      - Coarctation of aorta
      - Hypoplastic left heart
      - Tetralogy of Fallot
      - Ventricular septal defect
    additionalInfoNeeded:
      - Arrhythmia
      - Cardiomyopathy
CLINICAL_PHENOTYPES__NEUROLOGICAL:
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      - Ataxia
      - Brain imaging abnormality
      - Cerebral palsy
      - Developmental regression
      - Dystonia
      - Hypertonia
      - Hypotonia
      - Muscle weakness
      - Neural tube defect
      - Seizures
    additionalInfoNeeded:
      - Brain imaging abnormality
CLINICAL_PHENOTYPES__MUSCULOSKELETAL:
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      - Abnormality of limbs
      - Abnormal vertebral morphology
      - Flexion contracture
      - Polydactyly
      - Scoliosis
      - Syndactyly
      - Talipes equinovarus (club foot)
CLINICAL_PHENOTYPES__CUTANEOUS:
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      - Café au lait spots
      - Eczema
      - Hyperpigmentation of the skin
      - Hypopigmentation of the skin
CLINICAL_PHENOTYPES__GASTROINTESTINAL:
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    choices:
      - Aganglionic megacolon (Hirschsprung)
      - Anal atresia
      - Congential diaphragmatic hernia
      - Gastroschisis
      - Meconium ileus
      - Omphalocele
      - Pyloric stenosis
      - Tracheoesophageal fistul
CLINICAL_PHENOTYPES__GENITOURINARY:
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    choices:
      - Abnormal renal morphology
      - Ambiguous genitalia
      - Cryptorchidism
      - Hydronephrosis
      - Hypospadias
    additionalInfoNeeded:
      - Abnormal renal morphology
CLINICAL_PHENOTYPES__GROWTH:
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    choices:
      - Delayed puberty
      - Failure to thrive
      - Obesity
      - Precocious puberty
      - Short stature
      - Tall stature
CLINICAL_PHENOTYPES__OTHER:
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    choices: []