GENETIC COUNSELLING

Understanding what runs in the family.

A rare disease diagnosis often raises new questions — for you, for your children and for relatives. Genetic counselling turns those questions into clear information you can act on.

What genetic counselling covers

  • How a condition is inherited and who in the family may be at risk
  • Which genetic tests are available and what each can and cannot show
  • What a test result means — including uncertain results
  • Options for family planning, explained neutrally
  • How to talk about a diagnosis with children and relatives
  • Access to support groups and further information

Who it is for

Families with a diagnosis

You already have a diagnosis and want to understand what it means for your family.

Families without one

Symptoms run in the family but no condition has been named yet.

Relatives of a patient

You are well but a relative has a genetic condition and you want to understand your own risk.

Frequently asked questions

Medical review

Medical reviewer: To be confirmed before publication — no medical content on this page may go live without human medical review.

Review date: Pending  |  Next review: Pending

Sources: Content on this page must be verified against Ministry of Health and Family Welfare, ICMR, Department of Health Research, recognised Centres of Excellence, WHO or Orphanet guidance before publication.

Information on this page is for education and care navigation and does not replace consultation with a qualified healthcare professional.

Ask about genetic counselling

ACCORD Asha
13, Gaushala Rd, Ansal Villas
Satbari
New Delhi 110074
India

Medical emergency warning: ACCORD's website and contact channels are not emergency services. For a medical emergency, contact your nearest emergency department or emergency service.

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