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Monday, 5 October

NEET UG · Biology · Principles of Inheritance and Variation

Sex Determination and Genetic Disorders: NEET previous year questions

15 questions in ten years of NEET, in 9 of 10 papers. Pattern: Every year. Here is how it is asked and which ideas come back.

Asked in 10 years
15
about 1.4 per paper
Years asked
9/10
last asked 2026
Chance of a question next paper
84%
historical rate, how we compute it
Weighted estimate
1.3
model; history: 1.4 a paper on average, typically 1–3

Key findings

  1. 01

    Asked in 9 of 10 papers, 15 questions in all: #37 of 204 topics by ten-year total. It comes back every 1.1 years on average.

  2. 02

    54% of its questions since 2018 tested an idea never asked before; none repeated an idea from the year before.

  3. 03

    The most repeated idea is Down, Klinefelter and Turner Syndromes, asked 4 times (2019, 2023, 2026), usually as “count correct statements on a genetic disorder”.

  4. 04

    NEET has asked 0 of the 10 ideas in this topic; 0 have never been asked, directly or indirectly.

  5. 05

    Mostly asked as one-line MCQ (67%); 47% easy, 0% hard, and down from 1.6 to 1.0 questions a paper since 2024.

Questions per year

0242’171’182’191’200’213’223’231’241’251’26
Up to 2023
1.6
per paper
Since 2024
1.0
-0.7
Usual gap
1.1 yrs
between papers asking it
Swing
±0.8
questions, year to year

Revise first

Down, Klinefelter and Turner Syndromes (2019 2023 2026); Mendelian Disorders and Their Loci (2020 2024); Pedigree Carrier Probability (2025)

How it is asked

Difficulty, format and skill

Across all 15 questions on Sex Determination and Genetic Disorders since 2017.

Difficulty

QUESTIONS
78
  • Easy7 · 47%
  • Medium8 · 53%
  • Hard0 · 0%

Format

SHARE
  • One-line MCQ · 10 Q67%
  • Two statements · 1 Q7%
  • Numerical · 1 Q7%
  • Match the lists · 1 Q7%
  • Other · 1 Q7%
  • Figure-based · 1 Q7%

Skill tested

SHARE
  • Recall · 10 Q67%
  • Concept · 2 Q13%
  • Data or graph · 1 Q7%
  • Figure reading · 1 Q7%
  • Application · 1 Q7%

Repeats

New idea, or one asked before?

Each column is a paper. Blue questions tested an idea NEET had not asked before; navy ones went back to an idea from an earlier paper. 2017 is the first paper, so everything in it counts as new.

2
1
2
1
3
3
1
1
1
’17’18’19’20’21’22’23’24’25’26
  • Idea asked for the first time
  • Idea asked in an earlier paper

Coverage of the topic

NEET has asked 0 of the 10 ideas in this topic. 0 have never been asked yet.

10
  • Asked directly0 · 0%
  • Touched inside another question10 · 100%
  • Never asked0 · 0%

Ideas come from Lumi’s syllabus map of NCERT. A never-asked idea is not a safe skip: most new questions come from exactly these.

Drill down

Idea, year, question

Every idea NEET tested in this topic, with its ten papers. Open one to read the questions.

  • Repeated4 · 27%2
    • 2026 · Q138
      Given below are two statements: Statement I: Down's syndrome is caused by the absence of one of the X-chromosomes. Statement II: Turner's…

      easyTwo statements

    • 2023 · Q143
      Which of the following statements are correct about Klinefelter's Syndrome? A. This disorder was first described by Langdon Down (1866).…

      mediumOther

    • 2023 · Q180
      Broad palm with single palm crease is visible in a person suffering from-

      easyOne-line MCQ

    • 2019 · Q176
      What is the genetic disorder in which an individual has an overall masculine development, gynaecomastia, and is sterile ?

      easyOne-line MCQNew idea

  • Repeated2 · 13%
  • Repeated2 · 13%
  • Repeated2 · 13%
  • 1 · 7%
  • 1 · 7%
  • 1 · 7%
  • 1 · 7%
  • 1 · 7%

Squares are the ten papers, 2017 to 2026; darker means more questions. Share is of the level above.

Ideas

Every idea inside this topic

9 different ideas were tested; 4 came more than once.

  • Down, Klinefelter and Turner Syndromes4×

    count correct statements on a genetic disorder

    One-line MCQ · 11% next
  • Mendelian Disorders and Their Loci2×

    correct match on genetic disorders

    Match the lists · 6% next
  • X-linked Recessive Inheritance2×

    inheritance pattern of an x-linked trait

    One-line MCQ · 6% next
  • XO, XY and ZW Sex Determination2×

    identify group with sex determination type

    One-line MCQ · 6% next
  • Pedigree Carrier Probability1×

    numerical

    Numerical · 6% next
  • Pedigree Symbols1×

    identify pedigree symbol

    Figure-based · 4% next
  • Autosomal Dominant Disorders1×

    identify disorder by inheritance pattern

    One-line MCQ · 4% next
  • Aneuploidy and Non-disjunction1×

    identify disorder by cause

    One-line MCQ · 4% next
  • Thalassaemia versus Sickle-cell Anaemia1×

    true statement selection on genetic disorders

    One-line MCQ · 4% next

Chance next is the historical rate at which an idea with this record came back in the following paper. It is low for every idea, which is why learning the topic beats memorising past questions. All repeated ideas

Every question

Sex Determination and Genetic Disorders questions, year by year

The opening words of each question as it appeared in the official paper, with the idea it tested.

NEET 20261 question

  • Q138
    Given below are two statements: Statement I: Down's syndrome is caused by the absence of one of the X-chromosomes. Statement II: Turner's…

    Idea: Down, Klinefelter and Turner Syndromes

    EasyTwo statements

NEET 20251 question

  • Q152
    With the help of given pedigree, find out the probability for the birth of a child having no disease and being a carrier (has the disease…

    Idea: Pedigree Carrier Probability

    New ideaMediumNumerical · figure

NEET 20241 question

  • Q182
    Match List I with List II List-I | List-II A. Down's syndrome | I. 11th chromosome B. α-Thalassaemia | II. 'X' chromosome C.…

    Idea: Mendelian Disorders and Their Loci

    MediumMatch the lists

NEET 20233 questions

  • Q143
    Which of the following statements are correct about Klinefelter's Syndrome? A. This disorder was first described by Langdon Down (1866).…

    Idea: Down, Klinefelter and Turner Syndromes

    MediumOther
  • Q180
    Broad palm with single palm crease is visible in a person suffering from-

    Idea: Down, Klinefelter and Turner Syndromes

    EasyOne-line MCQ
  • Q185
    Which one of the following symbols represents mating between relatives in human pedigree analysis?

    Idea: Pedigree Symbols

    New ideaEasyFigure-based · figure

NEET 20223 questions

  • Q106
    XO type of sex determination can be found in :

    Idea: XO, XY and ZW Sex Determination

    EasyOne-line MCQ
  • Q144
    Which of the following occurs due to the presence of autosome linked dominant trait ?

    Idea: Autosomal Dominant Disorders

    New ideaMediumOne-line MCQ
  • Q198
    If a colour blind female marries a man whose mother was also colour blind, what are the chances of her progeny having colour blindness ?

    Idea: X-linked Recessive Inheritance

    MediumOne-line MCQ

NEET 20201 question

  • Q8
    Select the correct match.

    Idea: Mendelian Disorders and Their Loci

    New ideaMediumOne-line MCQ

NEET 20192 questions

  • Q121
    Select the incorrect statement.

    Idea: XO, XY and ZW Sex Determination

    New ideaMediumOne-line MCQ
  • Q176
    What is the genetic disorder in which an individual has an overall masculine development, gynaecomastia, and is sterile ?

    Idea: Down, Klinefelter and Turner Syndromes

    New ideaEasyOne-line MCQ

NEET 20181 question

  • Q159
    A woman has an X-linked condition on one of her X chromosomes. This chromosome can be inherited by

    Idea: X-linked Recessive Inheritance

    New ideaEasyOne-line MCQ

NEET 20172 questions

  • Q128
    A disease caused by an autosomal primary non-disjunction is

    Idea: Aneuploidy and Non-disjunction

    EasyOne-line MCQ
  • Q179
    Thalassemia and sickle cell anemia are caused due to a problem in globin molecule synthesis. Select the correct statement.

    Idea: Thalassaemia versus Sickle-cell Anaemia

    MediumOne-line MCQ

Questions from the official NEET UG papers published by NTA (CBSE before 2019). Topic and idea tags, counts and notes are Lumi’s.