UCCEDD Online Intake Form
Tell us about yourself:
Who may we thank for referring you to this form?
Please select...
Lynne Fogel-ODH
Amy Clawson
Jena Wells
Celia Schloemer
Michelle Schroeder
Hadia Khan
Ohiof2f.org
Ucucedd.org/family-support/
Nationwide Children’s Hospital
Cincinnati Children’s Hospital
Dayton Children’s Hospital
Akron Children’s Hospital
Rainbow Babies and Children’s Hospital
Cleveland Clinic Children’s Hospital
Other (Please explain)
Other
Adult Section
First Name
Last Name
Your Relationship to
Child with disability and/or special healthcare needs:
Please select...
Parent
Aunt/Uncle
Niece/Nephew
Cousin
Sibling
Grandparent
Social Worker
Client
Foster Parent
Legal Guardian
Other
Other Relationship Explanation
Mailing Street
City:
State
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County
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Adams
Allen
Ashland
Ashtabula
Athens
Auglaize
Belmont
Brown
Butler
Carroll
Champaign
Clark
Clermont
Clinton
Columbiana
Coshocton
Crawford
Cuyahoga
Darke
Defiance
Delaware
Erie
Fairfield
Fayette
Franklin
Fulton
Gallia
Geauga
Greene
Guernsey
Hamilton
Hancock
Hardin
Harrison
Henry
Highland
Hocking
Holmes
Huron
Jackson
Jefferson
Knox
Lake
Lawrence
Licking
Logan
Lorain
Lucas
Madison
Mahoning
Marion
Medina
Meigs
Mercer
Miami
Monroe
Montgomery
Morgan
Morrow
Muskingum
Noble
Ottawa
Paulding
Perry
Pickaway
Pike
Portage
Preble
Putnam
Richland
Ross
Sandusky
Scioto
Seneca
Shelby
Stark
Summit
Trumbull
Tuscarawas
Union
Van Wert
Vinton
Warren
Washington
Wayne
Williams
Wood
Wyandot
Out of State (Indiana)
Out of State (Kentucky)
Out of State (other state)
Email
Preferred Phone
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Home
Work
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Mobile
Work Phone
Best Time to Call
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Morning
Afternoon
Evening
Gender
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Female
Male
Trans
Non-binary
Other
Other Gender Explanation
Ethnicity
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Hispanic/Latino
Non Hispanic/Latino
Other
Other Ethnicity Explanation
Race
African-American/Black
American Indian/Native American/Alaskan Native
Asian
Caucasian/White
Native Hawaiian/Pacific Islander
Some other race
Two or more races
Prefer not to disclose
Race Explanation
Primary Language
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English
Spanish
Other
Other Language
Do you need an interpreter?
Yes
No
How did you hear about Ohio Family to Family/Parent to Parent?
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Friend
Family Member
School
Agency
Medical Practitioner
Other
If Other Please Explain
Tell us about the child/person with disability and/or special healthcare needs:
Child Section
Child First Name
Child Last Name
Child Gender
Please select...
Female
Male
Trans
Non-binary
Other
Child Other Gender Explanation
Date of Birth
Premature?
Yes
No
Weeks at birth?
NICU?
Yes
No
NICU Weeks?
Child Ethnicity
Please select...
Hispanic/Latino
Non Hispanic/Latino
Other
Child Other Ethnicity Explanation
Child Race
African-American/Black
American Indian/Native American/Alaskan Native
Asian
Caucasian/White
Native Hawaiian/Pacific Islander
Some other race
Two or more races
Prefer not to disclose
Child Race Explanation
Does the child have a diagnosis/diagnoses?
Yes
No
If so, when/where was diagnosis?
Who made the diagnosis?
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Healthcare Provider
School
Early Intervention
Other diagnosis not listed below:
Primary Diagnosis
Child Primary Diagnosis Category
:
Please select...
Autism Spectrum Disorder
Blood Disorder
Brain-related
Cancer & Tumor
Central Nervous System Disorder
Chromosomal Abnormality
Craniofacial & Dental
Ears & Hearing
Endocrine Disorder
Eyes & Vision
Feeding-Digestion-Weight
Gastrointestinal Disorder
Genetic Disorder
Genito-Urinary Disorder
Growth-Bone-Joint-Limb Disorder
Heart Disease & Disorder
Infections
Intellectual Disability
Learning Disability
Liver, Gall Bladder, Etc.
Lungs & Breathing
Mental Health Diagnosis
Metabolic Disease
Miscellaneous
Mitochondrial Disease
Muscles-Movement-Neuromuscular
Seizures & Epilepsy
Skin Disorder
Speech-Language
Substance Use-Abuse
Processing Disorders
Child Primary Diagnosis
:
Please select...
Autism
Aspergers Syndrome
Pervasive Developmental Disorder
Rett Syndrome
Agammaglobulinemia
Anemia
Aneurism
Blood Disorders
Factor IX Deficiency
Hemangioma
Hemoglobin H Disease
Hemophilia
Hypertension
Hypotension
Myelodysplastic Syndrome
Rh Disease
Sickle Cell Disease
Thalassemia
Thalassemia - Alpha
Thrombocytopenia
Acute disseminated encephalomyelitis (ADEM)
Agenesis of Corpus Callosum
Aicardi-Goutieres Syndrome
Binswanger's Disease
Cerebellum (Missing Part)
Colpocephaly
Corticobasal Degeneration
Empty Sella Syndrome (Turcica)
Encephalitis/Encephalopathy
Fahr's Disease
Gerstsmann Syndrome
Hyperekplexia (Stiff Man Syndrome)
Hypoxic-Ischemic Encephalopathy
Intraventricular Hemorrhage
Joubert Syndrome
Kernicterus
Leukodystrophy
Miller-Dieker Syndrome
Periventricular Leukomalacia
Stroke
Thalamic Pain Syndrome (Dejerine–Roussy syndrome)
Traumatic Brain Injury
Astrocytoma
Brain Tumor
Cancer
Cystic Hygroma
Ewings Sarcoma
Fibromatosis
Gangliocytoma
Glioblastoma Multiforme
Hemangiomas
Hodgkin's Disease
Leukemia
Lymphangioma
Lymphoma
Medulloblastoma
Melanoma
Meningioma
Myeloma, Multiple
Neuroblastoma
Neurofibromatosis
Ollier Disease
Pineoblastoma
Rhabdomyosarcoma
Vascular Hamartomas
Aicardi Syndrome
Alternating Hemiplegia
Anencephaly
Arnold-Chiari Syndrome
Caudal Regression Syndrome
Dandy-Walker Syndrome
Encephalocele
Holoprosencephaly
Hydranencephaly
Hydrocephalus
Hydromyelia
Lipomyelomeningocele
Lissencephaly
Macrocephaly
Megalencephaly
Microcephaly
Microgyria
Myelomeningocele
Myelomeningoencephalocele
Pachygyria
Polymicrogyria
Porencephaly
Schizencephaly
Spina Bifida
Stenosis, Spinal
Tethered Spinal Cord Syndrome
Alfi's Syndrome
Bloom Syndrome
Chromosomal Abnormalities
Chromosome 47XXX Karyotype
Chromosome 49XXXXY
Cri du Chat Syndrome (Le Jeune Syndrome)
Digeorge Syndrome
Down Syndrome
Down Syndrome: Mosaic Type
Klinefelter Syndrome XXY Syndrome
Pallister-Killian Mosaic Syndrome
Shprintzen Syndrome
Trichorhinophalangeal Syndrome (Langer-Giedion Syndrome (LGS))
Tripliod Syndrome
Turner Syndrome Mosaic
Turner Syndrome XO Syndrome
Velo-Cardio Facial Syndrome (deletion 22q11 syndrome; Shprintzen syndrome, Digeorge Syndrome)
Wolf-Hirschorn Syndrome
XXX Syndrome
XXYY Syndrome
XYY Syndrome (Jacob's Syndrome)
16p 11.2 deficiency
18q deletion
1p36 deletion
chromosome 22 deletion
8q deletion
Amelogenesis Imperfecta
Anodontia
Apert Syndrome
Cherubism
Cleft Lip and Palate
Craniofacial (Anomalies of Skull/Face
Crouzon Disease
Dubowitz Syndrome
Fronto-Nasal-Dysplasia
Goldenhar Syndrome
Hemifacial Microsomia
Macroglossia
Microsomia
Moebius Syndrome
Nager Syndrome
Oto-Palatal-Digital Syndrome
Pfeiffer Syndrome
Pierre-Robin Syndrome
Saethre-Chotzen Syndrome
Simpson Golabi Behmel Syndrome
Stickler Syndrome
Treacher Collins Syndrome
Trigonocephaly
Weaver Syndrome
Acoustic Neuroma
Atresia of the Ear
Branchio-Oto-Renal Syndrome
Cholesteotoma
Deaf
DeafBlind
Hearing Impaired, Partial
Meniere Disease
Microtia of the Ear
Otitis Media
Patulous Eustachian Tube
Sensorineural Hearing Loss
Stenotic Ear Canals
Waardenburg Syndrome
3-B Hydroxy Steroid Dehydorgenase Deficiency
Addisons Disease
Adrenal Gland Deficiency
Adrenal Hyperplasia
Adrenoleukodystrophy
Ahumada-del Castillo Syndrome
Apeced Syndrome (Whitaker syndrome)
Conn Syndrome
Desmolase Deficiency
Froelich's Syndrome (Frohlich)
Hydroxylase Deficiency
Hyperparathyroidism
Hypocortisolemia
Hypoparathyroidism
Panhypopituitarism
Shwachman Syndrome (Shwachman-Diamond)
Amblyopia
Anopthalmia
Blindness
Cataracts
Coats Disease
Coloboma
Cortical Visual Impairment
Glaucoma
Hypoplacia of eyes
Macular Degeneration
Microphthalmia
Myopia
Norrie Disease
Ocular Albinism
Optic Nerve Atrophy
Optic Nerve Coloboma
Optic Nerve Dysplasia
Optic Nerve Hypoplasia
Retinitis Pigmentosa (RP)
Retinoblastoma
Retinopathy of Prematurity (Retrolental Fibroplasia)
Septo-Optic Dysplasia
Strabismus
Usher's Syndrome
Anorexia Nervosa
Bulimia
Dysphagia (Difficulty in Swallowing)
Eosinophillia Esophagitis
Esophageal Atresia
Esophageal Dysmotility
Esophageal Stenosis
Feeding Disorder
Frey's Syndrome (Auriculotemporal)
Obesity
Pica
Polyphagia
Swallowing Disorder
Allergic Colitis
Celiac Disease
Colitis
Crohns Disease
Digestive Disorders
Dumping Syndrome
Duodenal Atresia
Gastritis
Gastroesophageal Reflux
Gastroparesis
Gastroschisis
Haddad Syndrome
Hirschsprungs Disease (Megacolon)
Intestinal Neuronal Dysplasia
Intestinal Pseudoobstruction
Jejunal Atresia
Malabsorption Syndrome
Motility Disorder
Necrotizing Enterocolitis
Omphalocele
Pyloric Stenosis
Short Bowel Syndrome
Waldmann Disease
Aarskog Syndrome
Angelman Syndrome
ATRX - alpha thalassemia/mental retardation syndrome X-linked
Bardet-Biedl Syndrome (Laurence-Moon-Biedi Syndrome)
Bassen-Kornzweig Syndrome (Abetalipoproteinenia)
Cerebro-Oculo-Facio-Skeletal Syndrome
CHARGE Disorder
Cockayne Syndrome
Coffin-Lowry Syndrome
Coffin-Siris Syndrome
Cohen Syndrome
Cornelia De Lange Syndrome
Ectodermal dysplasia
Ectrodactyly–ectodermal dysplasia–cleft syndrome
Filippin Syndrome
Fragile X Syndrome
Fraser Syndrome
Fryns Syndrome
Galloway Mowat Syndrome
Hypomelanosis of Ito
Kabuki Syndrome
Lowe Syndrome (Oculo-Cerebro-Renal Syndrome)
Marfan's Syndrome
Mowat-Wilson Syndrome
Opitz G/BBB syndrome
Opitz-Kaveggia syndrome (FG Syndrome)
Pallister-Hall Syndrome
Prader-Willi Syndrome
Rubinstein-Taybi Syndrome
Smith-Magenis Syndrome
Sturge-Weber Syndrome
Townes-Brocks Syndrome
Tuberous Sclerosis
Williams Syndrome
Abnormal Genitals
Ambiguous Genitalia
Androgen Insensitivity Syndrome
Anorectal Malformations
Cystinuria
Encopresis
Epispadias
Fanconi's Syndrome
Hermaphroditism
Hypospadias
Imperforate Anus
Nephrotic Syndrome
Neurogenic Bladder
Nocturia (Frequency Of Urination)
Polycystic Kidney Disease
Precocious Puberty
Prune Belly Syndrome
Pseudohermaphroditism
Rectal Malformation
Achondroplasia
Acrodysostosis (Arkless-Graham Syndrome)
Amniotic Band syndrome
Amputation
Arthritis
Arthrogryposis
Beckwith-Wiedemann Syndrome
Clubfoot
Clubhand
Congenital Deformity of Hip (Joint)
Dwarfism
Failure To Thrive
Fibula Abnormality
Growth Disorders
Growth Hormone Deficiency
Hand Deformity
Hip, Dislocated
Holt-Oram Syndrome
Intrauterine Growth Retardation
Klippel-Feil Syndrome
Kyphosis
Limb Disorders
Noonan Syndrome
Osteogenesis Imperfecta
Rickets
Russell-Silver Syndrome
Scoliosis
Split-Hand Deformity
Syndactyly
TAR Syndrome
Tibia Abnormality
Valgus Deformity of Ankles
Aortic Valve Stenosis
Arrhythmia
Atrial Septal Defects
Atrioventricular Canal Defect
Bradycardia
Cardiomegaly
Cardiomyopathy
Coarctation of the Aorta
Congenital Heart Disease
Congestive Heart Failure
Ebstein's Anomaly
Eisenmenger Syndrome
Endocardial Cushion Defect
Heterotaxy Syndrome
Hypoplastic Left Heart Syndrome
Hypoplastic Right Heart Syndrome
Long QT Syndrome
Mitral Valve Prolapse Syndrome
Patent Ductus Arteriosis
Tachycardia
Tetralogy of Fallot
Total Anomalous Pulmonary Venous Return
Transposition of the Great Arteries
Truncus Arteriosus
Ventricular Septal Defect (VSD)
Ventriculomegaly
AIDS (Acquired Immune Deficiency Synd.)
Chlamydia
Cholera
Cytomegalovirus Infection
Hand-Foot-Mouth Disease
Hepatitis B
Herpes Simplex
HIV
Human Papilloma Virus
Leptospirosis
Listeria
Lyme Disease
Malaria
Meningitis
Nocardia Infection
Papilloma
Polio
Q Fever
Rubella
Streptococcus
Syphillis, Congenital
Toxocariasis
Toxoplasmosis
Intellectual Disability (Mild)
Intellectual Disability (Moderate)
Intellectual Disability (Profound)
Intellectual Disability (Severe)
Attention Deficit Disorder
Attention Deficit Hyperactivity Disorder
Dyscalculia/Arithmetical Disorder
Dysgraphia
Dyslexia
Reactive Attention Disorder
Reading Disorder
Alagille Syndrome
Alpha-1-Antitrypsin Deficiency
Biliary Atresia
Budd-Chiari Syndrome
Caroli Syndrome
Cholangitis, Primary Sclerosing
Cholecystitis
Cholestasis
Cholesteryl Ester Storage Disease
Cirrhosis, Primary Biliary
Congenital Diaphragmatic Hernia
Dubin-Johnson Syndrome
Hyperbilirubinemia
Allergic Rhinitis
Asthma
Bronchopulmonary Dysplasia
Choanal Atresia
Chylothorax
Cystic Fibrosis
Diaphragmatic Hernia, Congenital
Hypoplastic Lungs
Hypoventilation Syndrome
Interstitial Lung Disease
Kartagener Syndrome
Laryngomalacia
Lung Disorders
Meconium Aspiration Syndrome
Pulmonary Atresia
Pulmonary Hypertension
Pulmonary Stenosis
Respiratory Distress Syndrome
Respiratory Syncytial Virus
Larygotracheal Stenosis
Tracheoesophageal Atresia
Tracheomalacia
Adjustment Disorder
Aggressive Behavior
Anxiety Disorder
Attachment Disorder
Behavior Disorder
Bi-Polar Disorder
Borderline Personality Disorder
Childhood Disintegrative Disorder (Heller's Syndrome)
Conduct Disorder
Depression
Intermittent Explosive Disorder
Obsessive Compulsive Disorder
Oppositional Disorder
Panic Anxiety Syndrome
Paranoia
Phobias
Post Traumatic Stress Syndrome
Reactive Attachment Disorder
Schizophrenia
Severe Separation Anxiety
Trichotillomania
Acrodermatitis Enteropathica
Biotinidase Deficiency
Carnitine Deficiency
Diabetes
Glutaric Aciduria
Glycogen Storage Disease
Hunter Syndrome (mucopolysaccharidosis II; mps-II)
Hurler Syndrome (mucopolysaccharidosis I; mps-I)
Hypothyroidism
Lesch-Nyhan Syndrome
Long-Chain Acyl-CoA Dehydrogenase (LCAD)
Maple Syrup Urine Disease
Medium-Chain Acyl-CoA Dehydrogen. (MCAD)
metachromatic leukodystrophy
Mucolipidosis
Niemann-Pick Disease
Phenylketonuria (PKU)
Pompe Disease
Purine Metabolic Disorders
Short-Chain Acyl-CoA Dehydrogenase(SCAD)
Tay-Sachs Disease
Tyrosinemia
Urea Cycle Metabolism Disorder
Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD)
Abuse, Emotional
Abuse, Physical
Abuse, Sexual
Allergies
Allergy (Food)
Allergy, Latex
Apnea
Auditory Defensive Disorder
Balance Disorder
Cushing Syndrome
Developmental Delay
Graft vs. Host Disease
Lead Poisoning
Lupus
Narcolepsy
Premature
Reyes Syndrome
Sensory Integration Deficit
Severe Combined Immunodeficiency
Shaken Baby Syndrome
Sudden Infant Death Syndrome
Tactile Defensive
Tardive Dyskinesia
Tourette Syndrome
Twin to Twin Transfusion Syndrome
Vater Syndrome (Vacterl Association)
Carboxylase Deficiency, Multiple
Dienoyl-CoA Reductase Deficiency
Kearns-Sayre Syndrome (mitochondrial myopathy)
L-3-Hydroxy-Acyl-CoA (LCHAD) Deficiency
Lactic Acidosis
Leighs Disease
Luft Disease
Mitochondrial Disorders
Mitochondrial Encephalapathic Lactic Acidosis (MELAS)
Mitochondrial Myopathy (Kearns-Sayre Syndrome)
Myoclonic Epilepsy and Ragged-Red Fibers (MERRF)
Neuropathy, ataxia, and retinitis pigmentosa (NARP)
Oxidative Phosphoralation Disease
Pearson Syndrome
Pyruvate Carboxylase Deficiency
Pyruvate Dehydrogenase Deficiency
Pyruvate Kinase Deficiency
Trifunctional Protein Deficiency
Wolfram Syndrome (DIDMOAD)
Ataxia
Bell's Palsy
Cerebral Palsy
Charcot-Marie-Tooth Disease
Congenital Myotonia
Dystonia
Erb's Palsy (Paralysis/Birth)
Fibromyalgia
Hemiparesis
Hemiplegia
Hypertonia
Hypotonia
Multiple Sclerosis
Muscular Dystrophy
Myasthenia Gravis
Myopathy
Myotonic Dystrophy
Nemaline Myopathy
Paralysis
Paraplegia
Quadriplegia
Spastic Diplegia
Spinal Muscular Atrophy (Werdnig-hoffmann Disease)
Torticollis
Epilepsy
Epilepsy, Grand Mal
Epilepsy, Petit Mal Status
Lafora Body Disease
Landau-Kleffner Syndrome
Lennox Gastaut Syndrome
Myoclonus
Ohtahara Syndrome
Rasmussen Syndrome
Seizure Disorder
West's Syndrome
Albinism
Crest Syndrome
Cutis Aplasia
Cutis Laxa
Eczema
Ehlers-Danlos Syndrome
Hives
Ichthyosis
Incontinentia Pigmenti
Leiner Disease
Lichen Planus
Nevus Syndrome
Proteus Syndrome
Psoriasis
Sweet Syndrome
Vitiligo
Ankyloglossia (Tongue Tied)
Aphasia
Apraxia, Speech
Dysfluency
Dyspraxia (Developmental Verbal)
Language Disorder, Expressive
Language Disorder, Receptive
Mutism
Oral Expressive Dyspraxia
Spasmodic Dysphonia
Speech Delay
Vocal Cord Paralysis
Addiction, Alcohol
Addiction, Drug
Dilantin Embryopathy
Drug Dependence
Fetal Alcohol Effects
Fetal Alcohol Syndrome
Auditory Processing Disorder
Sensory Processing Disorders
Visual Processing Disorder
Secondary Diagnosis
Child Secondary Diagnosis Category
:
Please select...
Autism Spectrum Disorder
Blood Disorder
Brain-related
Cancer & Tumor
Central Nervous System Disorder
Chromosomal Abnormality
Craniofacial & Dental
Ears & Hearing
Endocrine Disorder
Eyes & Vision
Feeding-Digestion-Weight
Gastrointestinal Disorder
Genetic Disorder
Genito-Urinary Disorder
Growth-Bone-Joint-Limb Disorder
Heart Disease & Disorder
Infections
Intellectual Disability
Learning Disability
Liver, Gall Bladder, Etc.
Lungs & Breathing
Mental Health Diagnosis
Metabolic Disease
Miscellaneous
Mitochondrial Disease
Muscles-Movement-Neuromuscular
Seizures & Epilepsy
Skin Disorder
Speech-Language
Substance Use-Abuse
Processing Disorders
Child Secondary Diagnosis
:
Please select...
Autism
Aspergers Syndrome
Pervasive Developmental Disorder
Rett Syndrome
Agammaglobulinemia
Anemia
Aneurism
Blood Disorders
Factor IX Deficiency
Hemangioma
Hemoglobin H Disease
Hemophilia
Hypertension
Hypotension
Myelodysplastic Syndrome
Rh Disease
Sickle Cell Disease
Thalassemia
Thalassemia - Alpha
Thrombocytopenia
Acute disseminated encephalomyelitis (ADEM)
Agenesis of Corpus Callosum
Aicardi-Goutieres Syndrome
Binswanger's Disease
Cerebellum (Missing Part)
Colpocephaly
Corticobasal Degeneration
Empty Sella Syndrome (Turcica)
Encephalitis/Encephalopathy
Fahr's Disease
Gerstsmann Syndrome
Hyperekplexia (Stiff Man Syndrome)
Hypoxic-Ischemic Encephalopathy
Intraventricular Hemorrhage
Joubert Syndrome
Kernicterus
Leukodystrophy
Miller-Dieker Syndrome
Periventricular Leukomalacia
Stroke
Thalamic Pain Syndrome (Dejerine–Roussy syndrome)
Traumatic Brain Injury
Astrocytoma
Brain Tumor
Cancer
Cystic Hygroma
Ewings Sarcoma
Fibromatosis
Gangliocytoma
Glioblastoma Multiforme
Hemangiomas
Hodgkin's Disease
Leukemia
Lymphangioma
Lymphoma
Medulloblastoma
Melanoma
Meningioma
Myeloma, Multiple
Neuroblastoma
Neurofibromatosis
Ollier Disease
Pineoblastoma
Rhabdomyosarcoma
Vascular Hamartomas
Aicardi Syndrome
Alternating Hemiplegia
Anencephaly
Arnold-Chiari Syndrome
Caudal Regression Syndrome
Dandy-Walker Syndrome
Encephalocele
Holoprosencephaly
Hydranencephaly
Hydrocephalus
Hydromyelia
Lipomyelomeningocele
Lissencephaly
Macrocephaly
Megalencephaly
Microcephaly
Microgyria
Myelomeningocele
Myelomeningoencephalocele
Pachygyria
Polymicrogyria
Porencephaly
Schizencephaly
Spina Bifida
Stenosis, Spinal
Tethered Spinal Cord Syndrome
Alfi's Syndrome
Bloom Syndrome
Chromosomal Abnormalities
Chromosome 47XXX Karyotype
Chromosome 49XXXXY
Cri du Chat Syndrome (Le Jeune Syndrome)
Digeorge Syndrome
Down Syndrome
Down Syndrome: Mosaic Type
Klinefelter Syndrome XXY Syndrome
Pallister-Killian Mosaic Syndrome
Shprintzen Syndrome
Trichorhinophalangeal Syndrome (Langer-Giedion Syndrome (LGS))
Tripliod Syndrome
Turner Syndrome Mosaic
Turner Syndrome XO Syndrome
Velo-Cardio Facial Syndrome (deletion 22q11 syndrome; Shprintzen syndrome, Digeorge Syndrome)
Wolf-Hirschorn Syndrome
XXX Syndrome
XXYY Syndrome
XYY Syndrome (Jacob's Syndrome)
16p 11.2 deficiency
18q deletion
1p36 deletion
chromosome 22 deletion
8q deletion
Amelogenesis Imperfecta
Anodontia
Apert Syndrome
Cherubism
Cleft Lip and Palate
Craniofacial (Anomalies of Skull/Face
Crouzon Disease
Dubowitz Syndrome
Fronto-Nasal-Dysplasia
Goldenhar Syndrome
Hemifacial Microsomia
Macroglossia
Microsomia
Moebius Syndrome
Nager Syndrome
Oto-Palatal-Digital Syndrome
Pfeiffer Syndrome
Pierre-Robin Syndrome
Saethre-Chotzen Syndrome
Simpson Golabi Behmel Syndrome
Stickler Syndrome
Treacher Collins Syndrome
Trigonocephaly
Weaver Syndrome
Acoustic Neuroma
Atresia of the Ear
Branchio-Oto-Renal Syndrome
Cholesteotoma
Deaf
DeafBlind
Hearing Impaired, Partial
Meniere Disease
Microtia of the Ear
Otitis Media
Patulous Eustachian Tube
Sensorineural Hearing Loss
Stenotic Ear Canals
Waardenburg Syndrome
3-B Hydroxy Steroid Dehydorgenase Deficiency
Addisons Disease
Adrenal Gland Deficiency
Adrenal Hyperplasia
Adrenoleukodystrophy
Ahumada-del Castillo Syndrome
Apeced Syndrome (Whitaker syndrome)
Conn Syndrome
Desmolase Deficiency
Froelich's Syndrome (Frohlich)
Hydroxylase Deficiency
Hyperparathyroidism
Hypocortisolemia
Hypoparathyroidism
Panhypopituitarism
Shwachman Syndrome (Shwachman-Diamond)
Amblyopia
Anopthalmia
Blindness
Cataracts
Coats Disease
Coloboma
Cortical Visual Impairment
Glaucoma
Hypoplacia of eyes
Macular Degeneration
Microphthalmia
Myopia
Norrie Disease
Ocular Albinism
Optic Nerve Atrophy
Optic Nerve Coloboma
Optic Nerve Dysplasia
Optic Nerve Hypoplasia
Retinitis Pigmentosa (RP)
Retinoblastoma
Retinopathy of Prematurity (Retrolental Fibroplasia)
Septo-Optic Dysplasia
Strabismus
Usher's Syndrome
Anorexia Nervosa
Bulimia
Dysphagia (Difficulty in Swallowing)
Eosinophillia Esophagitis
Esophageal Atresia
Esophageal Dysmotility
Esophageal Stenosis
Feeding Disorder
Frey's Syndrome (Auriculotemporal)
Obesity
Pica
Polyphagia
Swallowing Disorder
Allergic Colitis
Celiac Disease
Colitis
Crohns Disease
Digestive Disorders
Dumping Syndrome
Duodenal Atresia
Gastritis
Gastroesophageal Reflux
Gastroparesis
Gastroschisis
Haddad Syndrome
Hirschsprungs Disease (Megacolon)
Intestinal Neuronal Dysplasia
Intestinal Pseudoobstruction
Jejunal Atresia
Malabsorption Syndrome
Motility Disorder
Necrotizing Enterocolitis
Omphalocele
Pyloric Stenosis
Short Bowel Syndrome
Waldmann Disease
Aarskog Syndrome
Angelman Syndrome
ATRX - alpha thalassemia/mental retardation syndrome X-linked
Bardet-Biedl Syndrome (Laurence-Moon-Biedi Syndrome)
Bassen-Kornzweig Syndrome (Abetalipoproteinenia)
Cerebro-Oculo-Facio-Skeletal Syndrome
CHARGE Disorder
Cockayne Syndrome
Coffin-Lowry Syndrome
Coffin-Siris Syndrome
Cohen Syndrome
Cornelia De Lange Syndrome
Ectodermal dysplasia
Ectrodactyly–ectodermal dysplasia–cleft syndrome
Filippin Syndrome
Fragile X Syndrome
Fraser Syndrome
Fryns Syndrome
Galloway Mowat Syndrome
Hypomelanosis of Ito
Kabuki Syndrome
Lowe Syndrome (Oculo-Cerebro-Renal Syndrome)
Marfan's Syndrome
Mowat-Wilson Syndrome
Opitz G/BBB syndrome
Opitz-Kaveggia syndrome (FG Syndrome)
Pallister-Hall Syndrome
Prader-Willi Syndrome
Rubinstein-Taybi Syndrome
Smith-Magenis Syndrome
Sturge-Weber Syndrome
Townes-Brocks Syndrome
Tuberous Sclerosis
Williams Syndrome
Abnormal Genitals
Ambiguous Genitalia
Androgen Insensitivity Syndrome
Anorectal Malformations
Cystinuria
Encopresis
Epispadias
Fanconi's Syndrome
Hermaphroditism
Hypospadias
Imperforate Anus
Nephrotic Syndrome
Neurogenic Bladder
Nocturia (Frequency Of Urination)
Polycystic Kidney Disease
Precocious Puberty
Prune Belly Syndrome
Pseudohermaphroditism
Rectal Malformation
Achondroplasia
Acrodysostosis (Arkless-Graham Syndrome)
Amniotic Band syndrome
Amputation
Arthritis
Arthrogryposis
Beckwith-Wiedemann Syndrome
Clubfoot
Clubhand
Congenital Deformity of Hip (Joint)
Dwarfism
Failure To Thrive
Fibula Abnormality
Growth Disorders
Growth Hormone Deficiency
Hand Deformity
Hip, Dislocated
Holt-Oram Syndrome
Intrauterine Growth Retardation
Klippel-Feil Syndrome
Kyphosis
Limb Disorders
Noonan Syndrome
Osteogenesis Imperfecta
Rickets
Russell-Silver Syndrome
Scoliosis
Split-Hand Deformity
Syndactyly
TAR Syndrome
Tibia Abnormality
Valgus Deformity of Ankles
Aortic Valve Stenosis
Arrhythmia
Atrial Septal Defects
Atrioventricular Canal Defect
Bradycardia
Cardiomegaly
Cardiomyopathy
Coarctation of the Aorta
Congenital Heart Disease
Congestive Heart Failure
Ebstein's Anomaly
Eisenmenger Syndrome
Endocardial Cushion Defect
Heterotaxy Syndrome
Hypoplastic Left Heart Syndrome
Hypoplastic Right Heart Syndrome
Long QT Syndrome
Mitral Valve Prolapse Syndrome
Patent Ductus Arteriosis
Tachycardia
Tetralogy of Fallot
Total Anomalous Pulmonary Venous Return
Transposition of the Great Arteries
Truncus Arteriosus
Ventricular Septal Defect (VSD)
Ventriculomegaly
AIDS (Acquired Immune Deficiency Synd.)
Chlamydia
Cholera
Cytomegalovirus Infection
Hand-Foot-Mouth Disease
Hepatitis B
Herpes Simplex
HIV
Human Papilloma Virus
Leptospirosis
Listeria
Lyme Disease
Malaria
Meningitis
Nocardia Infection
Papilloma
Polio
Q Fever
Rubella
Streptococcus
Syphillis, Congenital
Toxocariasis
Toxoplasmosis
Intellectual Disability (Mild)
Intellectual Disability (Moderate)
Intellectual Disability (Profound)
Intellectual Disability (Severe)
Attention Deficit Disorder
Attention Deficit Hyperactivity Disorder
Dyscalculia/Arithmetical Disorder
Dysgraphia
Dyslexia
Reactive Attention Disorder
Reading Disorder
Alagille Syndrome
Alpha-1-Antitrypsin Deficiency
Biliary Atresia
Budd-Chiari Syndrome
Caroli Syndrome
Cholangitis, Primary Sclerosing
Cholecystitis
Cholestasis
Cholesteryl Ester Storage Disease
Cirrhosis, Primary Biliary
Congenital Diaphragmatic Hernia
Dubin-Johnson Syndrome
Hyperbilirubinemia
Allergic Rhinitis
Asthma
Bronchopulmonary Dysplasia
Choanal Atresia
Chylothorax
Cystic Fibrosis
Diaphragmatic Hernia, Congenital
Hypoplastic Lungs
Hypoventilation Syndrome
Interstitial Lung Disease
Kartagener Syndrome
Laryngomalacia
Lung Disorders
Meconium Aspiration Syndrome
Pulmonary Atresia
Pulmonary Hypertension
Pulmonary Stenosis
Respiratory Distress Syndrome
Respiratory Syncytial Virus
Larygotracheal Stenosis
Tracheoesophageal Atresia
Tracheomalacia
Adjustment Disorder
Aggressive Behavior
Anxiety Disorder
Attachment Disorder
Behavior Disorder
Bi-Polar Disorder
Borderline Personality Disorder
Childhood Disintegrative Disorder (Heller's Syndrome)
Conduct Disorder
Depression
Intermittent Explosive Disorder
Obsessive Compulsive Disorder
Oppositional Disorder
Panic Anxiety Syndrome
Paranoia
Phobias
Post Traumatic Stress Syndrome
Reactive Attachment Disorder
Schizophrenia
Severe Separation Anxiety
Trichotillomania
Acrodermatitis Enteropathica
Biotinidase Deficiency
Carnitine Deficiency
Diabetes
Glutaric Aciduria
Glycogen Storage Disease
Hunter Syndrome (mucopolysaccharidosis II; mps-II)
Hurler Syndrome (mucopolysaccharidosis I; mps-I)
Hypothyroidism
Lesch-Nyhan Syndrome
Long-Chain Acyl-CoA Dehydrogenase (LCAD)
Maple Syrup Urine Disease
Medium-Chain Acyl-CoA Dehydrogen. (MCAD)
metachromatic leukodystrophy
Mucolipidosis
Niemann-Pick Disease
Phenylketonuria (PKU)
Pompe Disease
Purine Metabolic Disorders
Short-Chain Acyl-CoA Dehydrogenase(SCAD)
Tay-Sachs Disease
Tyrosinemia
Urea Cycle Metabolism Disorder
Very Long Chain Acyl-CoA Dehydrogenase Deficiency (VLCAD)
Abuse, Emotional
Abuse, Physical
Abuse, Sexual
Allergies
Allergy (Food)
Allergy, Latex
Apnea
Auditory Defensive Disorder
Balance Disorder
Cushing Syndrome
Developmental Delay
Graft vs. Host Disease
Lead Poisoning
Lupus
Narcolepsy
Premature
Reyes Syndrome
Sensory Integration Deficit
Severe Combined Immunodeficiency
Shaken Baby Syndrome
Sudden Infant Death Syndrome
Tactile Defensive
Tardive Dyskinesia
Tourette Syndrome
Twin to Twin Transfusion Syndrome
Vater Syndrome (Vacterl Association)
Carboxylase Deficiency, Multiple
Dienoyl-CoA Reductase Deficiency
Kearns-Sayre Syndrome (mitochondrial myopathy)
L-3-Hydroxy-Acyl-CoA (LCHAD) Deficiency
Lactic Acidosis
Leighs Disease
Luft Disease
Mitochondrial Disorders
Mitochondrial Encephalapathic Lactic Acidosis (MELAS)
Mitochondrial Myopathy (Kearns-Sayre Syndrome)
Myoclonic Epilepsy and Ragged-Red Fibers (MERRF)
Neuropathy, ataxia, and retinitis pigmentosa (NARP)
Oxidative Phosphoralation Disease
Pearson Syndrome
Pyruvate Carboxylase Deficiency
Pyruvate Dehydrogenase Deficiency
Pyruvate Kinase Deficiency
Trifunctional Protein Deficiency
Wolfram Syndrome (DIDMOAD)
Ataxia
Bell's Palsy
Cerebral Palsy
Charcot-Marie-Tooth Disease
Congenital Myotonia
Dystonia
Erb's Palsy (Paralysis/Birth)
Fibromyalgia
Hemiparesis
Hemiplegia
Hypertonia
Hypotonia
Multiple Sclerosis
Muscular Dystrophy
Myasthenia Gravis
Myopathy
Myotonic Dystrophy
Nemaline Myopathy
Paralysis
Paraplegia
Quadriplegia
Spastic Diplegia
Spinal Muscular Atrophy (Werdnig-hoffmann Disease)
Torticollis
Epilepsy
Epilepsy, Grand Mal
Epilepsy, Petit Mal Status
Lafora Body Disease
Landau-Kleffner Syndrome
Lennox Gastaut Syndrome
Myoclonus
Ohtahara Syndrome
Rasmussen Syndrome
Seizure Disorder
West's Syndrome
Albinism
Crest Syndrome
Cutis Aplasia
Cutis Laxa
Eczema
Ehlers-Danlos Syndrome
Hives
Ichthyosis
Incontinentia Pigmenti
Leiner Disease
Lichen Planus
Nevus Syndrome
Proteus Syndrome
Psoriasis
Sweet Syndrome
Vitiligo
Ankyloglossia (Tongue Tied)
Aphasia
Apraxia, Speech
Dysfluency
Dyspraxia (Developmental Verbal)
Language Disorder, Expressive
Language Disorder, Receptive
Mutism
Oral Expressive Dyspraxia
Spasmodic Dysphonia
Speech Delay
Vocal Cord Paralysis
Addiction, Alcohol
Addiction, Drug
Dilantin Embryopathy
Drug Dependence
Fetal Alcohol Effects
Fetal Alcohol Syndrome
Auditory Processing Disorder
Sensory Processing Disorders
Visual Processing Disorder
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