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Accepting patients
Who is Dr. Weaver, Clinical Geneticist in Cincinnati, OH?
Dr. Kathryn Weaver, MD is a Clinical Geneticist, who primarily practices in Cincinnati, OH. She is board certified. Dr. Weaver graduated from University of Alabama School of Medicine and completed her residency at Cincinnati Children's Hospital Medical Center Program. Dr. Weaver is fluent in English, and is currently seeing new patients. Dr. Weaver’s practice accepts Medicare, UnitedHealthcare and other major insurance plans. To book an appointment or to confirm insurance options, please call Dr. Weaver’s office at (513) 636-4760.
Where did Dr. Weaver go to medical school and complete their residency?
Residency: Cincinnati Children's Hospital Medical Center Program
Medical School: University of Alabama School of Medicine
What languages does Dr. Weaver speak?
Dr. Weaver and their clinical team can communicate with patients in the following languages:
English
What conditions does Dr. Weaver treat?
As a Clinical Geneticist, Dr. Weaver diagnoses, treats, and manages a wide range of conditions. This condition information is derived from anonymized insurance claims and highlights the medical conditions most commonly treated by Dr. Weaver. It provides insight into the doctor’s areas of experience and expertise based on real-world patient encounters from the past two years, updated quarterly.
Also known as:
- Other Birth Defects Causing Short Stature
- Other Genetic Syndrome
- Birth Defects
- Rare Short Stature Syndromes
- Uncommon Dwarfism
- Rare Birth Defect Syndromes
- Uncommon Congenital Syndromes
ICD-10 Codes:
- Q8719: Other congenital malformation syndromes predominantly associated with short stature
- Q8789: Other specified congenital malformation syndromes, not elsewhere classified
Also known as:
- Niemann-Pick Disease
- Niemann-Pick Disease Type B
- Niemann-Pick Disease Type A/B
- Niemann-Pick Disease Type C
- Genetic Brain Disorder
- Niemann-Pick disease
- NPD
- Sphingomyelin lipidosis
- Lysosomal storage disorder
- NPD type B
- Acid sphingomyelinase deficiency
- ASM deficiency
- Niemann-Pick type A and B
- NPD type C
- NPC disease
- Cholesterol storage disease
ICD-10 Codes:
- E75249: Niemann-Pick disease, unspecified
- E75241: Niemann-Pick disease type B
- E75248: Other Niemann-Pick disease
- E75244: Niemann-Pick disease type A/B
- E75242: Niemann-Pick disease type C
Also known as:
- Neurofibromatosis Type 1
- Neurofibromatosis
- Neurofibromatosis type 1
- NF1
- Von Recklinghausen disease
- Peripheral neurofibromatosis
ICD-10 Codes:
- Q8501: Neurofibromatosis, type 1
Also known as:
- Marfan Syndrome
- MFS
- Genetic connective tissue disorder
- Fibrillinopathy
ICD-10 Codes:
- Q8740: Marfan syndrome, unspecified
Also known as:
- Sunken Chest
- Birth Defects
- Pectus Excavatum
- Funnel Chest
- Concave Chest
ICD-10 Codes:
- Q676: Pectus excavatum
Also known as:
- Williams Syndrome
- Other Chromosomal Abnormality
- Genetic Disorder
- Williams-Beuren Syndrome
- WS
- Elfin Facies Syndrome
- Rare Chromosome Disorder
- Atypical Chromosomal Condition
- Genetic Chromosome Problem
ICD-10 Codes:
- Q9382: Williams syndrome
- Q998: Other specified chromosome abnormalities
Also known as:
- Aortic Ectasia
- Aortic Widening
- Dilated Aorta
- Aortic Dilation
ICD-10 Codes:
- I77819: Aortic ectasia, unspecified site
Also known as:
- Pigeon Chest
- Birth Defects
- Pectus Carinatum
- Keel Chest
- Protruding Breastbone
ICD-10 Codes:
- Q677: Pectus carinatum
Also known as:
- Other Speech Problems
- Speech and Communication Disorder
- Unspecified speech issues
- Speech difficulties
- Communication problems
ICD-10 Codes:
- R4789: Other speech disturbances
Also known as:
- Family History of Heart Disease
- Family History
- Heart Disease
- Hereditary heart disease risk
- Genetic predisposition to heart problems
- Heart conditions in the family
ICD-10 Codes:
- Z8249: Family history of ischemic heart disease and other diseases of the circulatory system
Also known as:
- Other Muscle and Bone System Symptoms
- Movement Disorder
- Muscle Disorder
- Unusual Musculoskeletal Symptoms
- Muscle and Joint Problems
- Bone and Muscle Issues
ICD-10 Codes:
- R29898: Other symptoms and signs involving the musculoskeletal system
Also known as:
- Hand or Finger Deformity at Birth
- Birth Defects
- Congenital Hand Malformation
- Finger Birth Defect
- Baby Hand Anomaly
ICD-10 Codes:
- Q681: Congenital deformity of finger(s) and hand
Also known as:
- Generalized Muscle Weakness
- Muscle Disorder
- Overall Body Weakness
- Widespread Muscle Weakness
- Systemic Muscle Weakness
ICD-10 Codes:
- M6281: Muscle weakness (generalized)
Also known as:
- Autism
- Autism Spectrum Disorder
- Classic Autism', 'Kanner's Syndrome
- Severe Autism
ICD-10 Codes:
- F840: Autistic disorder
Which procedures does Dr. Weaver perform as a Clinical Geneticist?
As a Clinical Geneticist, procedures performed by a Dr. Kathryn Weaver may include:
- Biochemical Genetics Consultation
- Biochemical Genetics Follow Up
- Enzyme Replacement Therapy
- Genetic Testing
- Metabolic Assessment and Management
For detailed information, please contact Dr. Weaver's office.
Does Dr. Weaver accept my insurance?
Dr. Weaver accepts most major insurance plans. Important: Please call our office at (513) 636-4760 before your appointment to verify that your specific plan and network are accepted.
What insurance plans does Dr. Weaver accept in Cincinnati, OH?
Dr. Weaver in Cincinnati, OH accepts plans from many carriers. While this list is updated regularly, it is not a guarantee of coverage.
Top Insurances
CareSource
Centene
CVS Health (formerly Aetna)
Elevance Health Inc. (formerly Anthem)
Express Scripts
Humana
Medical Mutual
State of Kentucky
State of Ohio
UnitedHealthcare
View All Insurances
Where is Dr. Weaver's office located?
Dr. Kathryn Weaver's Primary Practice
3333 Burnet Ave # 4006
Cincinnati, OH 45229
(513) 636-4760
What is Dr. Weaver's NPI number?An National Provider Identifier (NPI) is a unique ID number that identifies doctors and healthcare providers nationwide.
Dr. Weaver's National Provider Identifier (NPI) number is 1003050998.
What common questions do patients ask about Dr. Weaver?
Here are answers to patients Frequently Asked Questions (FAQ’s) about Dr. Weaver
What is Dr. Kathryn Weaver's specialty?
Dr. Weaver is a Clinical Geneticist near Cincinnati, OH. A clinical geneticist is adept at offering thorough diagnostic, management, and counseling services for genetic disorders. Contact Dr. Weaver to book an appointment today.
Is this Dr. Kathryn Weaver affiliated with a ranked Castle Connolly Top Hospital?
No, Weaver is not affiliated with a Castle Connolly Top Hospital, but is affiliated with the following hospitals: Cincinnati Childrens - Burnet Campus. Castle Connolly Top Hospitals are identified through a rigorous peer nomination process, evaluating factors like patient outcomes, quality of care, and expertise. The list recognizes hospitals that excel in 20 or more specific medical procedures, representing the top 25% nationwide. Castle Connolly Top Hospitals
Where can I learn more about Clinical Geneticist?
Explore Clinical Geneticist with insights from trusted medical experts on EverydayHealth.com, where you'll find the most relevant content and helpful condition guides for up-to date information about symptoms, causes, diagnosis, treatment and more. See all our health guides to find trusted information on medical conditions from our experts at Everyday Health.
Is Kathryn Weaver accepting new patients in Cincinnati, OH?
Yes, Dr. Kathryn Weaver is accepting new patients at this time.
Does Dr. Kathryn Weaver offer online booking?
Please contact Dr. Weaver's office at (513) 636-4760 for information about online booking, telehealth, or to schedule an appointment.
How can I make an appointment with Kathryn Weaver?
Please contact Dr. Weaver's office at (513) 636-4760 for information regarding telehealth appointment availability or for scheduling assistance.
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