Written by students who passed Immediately available after payment Read online or as PDF Wrong document? Swap it for free 4.6 TrustPilot
logo-home
Document preview thumbnail
Preview 2 out of 8 pages
Exam (elaborations)

ABGC Board Study Inheritance Patterns with Complete Solutions

Document preview thumbnail
Preview 2 out of 8 pages

ABGC Board Study Inheritance Patterns with Complete Solutions

Content preview

ABGC Board Study Inheritance Patterns
with Complete Solutions
22q11.2 deletion syndrome - ANSWER-microdeletion

5 alpha reductase deficiency - ANSWER-autosomal recessive

achondrogenesis COL2A1 - ANSWER-autosomal dominant

achondrogenesis TRIP11, SLC26A2 - ANSWER-autosomal recessive

achondroplasia - ANSWER-autosomal dominant

Adelaide (Muenke) - ANSWER-autosomal dominant

Agammaglobulinemia (Bruton) - ANSWER-X-linked

Alagille - ANSWER-autosomal dominant

Alpha anti-trypsin deficiency - ANSWER-autosomal codominant

Alport 15% COL4A3/4 - ANSWER-autosomal recessive

Alport 80% COL4A5 - ANSWER-X-linked

Alstrom - ANSWER-autosomal recessive

amyotrophic lateral sclerosis (ALS) - ANSWER-autosomal dominant

Angelman - ANSWER-imprinting

Aniridia - ANSWER-autosomal dominant

Antley Bixler - ANSWER-autosomal recessive

Apert - ANSWER-autosomal dominant

Ataxia telangiectasia - ANSWER-autosomal recessive

BAP1 syndrome - ANSWER-autosomal dominant

Bardet Biedl - ANSWER-autosomal recessive

Becker muscular dystrophy - ANSWER-X-linked

, Birt Hogg Dube - ANSWER-autosomal dominant

Branchio-oto-renal syndrome - ANSWER-autosomal dominant

Cardiofaciocutaneous syndrome - ANSWER-autosomal dominant

Carney complex - ANSWER-autosomal dominant

Charcot Marie Tooth GJB1 - ANSWER-X-linked

Charcot Marie Tooth MFN2 - ANSWER-autosomal dominant

Charcot Marie Tooth PMP22 - ANSWER-microduplication

CHARGE - ANSWER-autosomal dominant

Chediak-Higashi syndrome - ANSWER-autosomal recessive

Citrullinemia - ANSWER-autosomal recessive

Classical Ehlers-Danlos syndrome - ANSWER-autosomal dominant

congenital adrenal hyperplasia - ANSWER-autosomal recessive

Congenital contractural arachnodactyly (Beals syndrome) - ANSWER-autosomal
dominant

connexion-26-related hearing loss - ANSWER-autosomal recessive

Cornelia de Lange - ANSWER-AD or X-linked

Costello - ANSWER-autosomal dominant

Cowden syndrome - ANSWER-autosomal dominant

Crouzon - ANSWER-autosomal dominant

Cystic fibrosis - ANSWER-autosomal recessive

Cystinosis - ANSWER-autosomal recessive

Denys-Drash syndrome - ANSWER-autosomal dominant

DICER1 syndrome - ANSWER-autosomal dominant

Document information

Uploaded on
January 18, 2025
Number of pages
8
Written in
2024/2025
Type
Exam (elaborations)
Contains
Questions & answers
$11.79

Wrong document? Swap it for free Within 14 days of purchase and before downloading, you can choose a different document. You can simply spend the amount again.
Written by students who passed
Immediately available after payment
Read online or as PDF

Seller avatar
Reputation scores are based on the amount of documents a seller has sold for a fee and the reviews they have received for those documents. There are three levels: Bronze, Silver and Gold. The better the reputation, the more your can rely on the quality of the sellers work.
LUCKYSTAR2022
3.4
(161)
Sold
925
Followers
725
Items
9640
Last sold
1 week ago


Why students choose Stuvia

Created by fellow students, verified by reviews

Quality you can trust: written by students who passed their tests and reviewed by others who've used these notes.

Didn't get what you expected? Choose another document

No worries! You can instantly pick a different document that better fits what you're looking for.

Pay as you like, start learning right away

No subscription, no commitments. Pay the way you're used to via credit card and download your PDF document instantly.

Student with book image

“Bought, downloaded, and aced it. It really can be that simple.”

Alisha Student

Working on your references?

Create accurate citations in APA, MLA and Harvard with our free citation generator.

Working on your references?

Frequently asked questions