Study Guides/Biology/Bombay Blood Group — What Is hh Phenotype and Why It Is Rare
Study Guide · Biology

Bombay Blood Group (hh Phenotype) — The Rarest Blood Type

The Bombay blood group (also known as hh phenotype or Oh blood group) is an extremely rare blood type first discovered in Mumbai (Bombay), India in 1952 by Dr. Y.M. Bhende. People with the Bombay blood group lack the H antigen on their red blood cells — the H antigen is the precursor to the A and B antigens of the ABO blood group system. Without the H antigen, neither A nor B antigens can be formed, making this group compatible only with other Bombay blood group donors.

Question (Click to Flip)

What is the Bombay blood group?

Answer

The Bombay blood group (hh phenotype / Oh blood group) is an extremely rare blood type where the person lacks the H antigen on their red blood cells. It was first discovered in 1952 in Bombay (Mumbai) by Dr. Y.M. Bhende. People with this group cannot donate or receive blood from any standard ABO group.

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Key Facts

Bombay blood group (hh phenotype / Oh group) lacks the H antigen on red blood cells.

Discovered in 1952 in Bombay (Mumbai) by Dr. Y.M. Bhende.

All other ABO blood groups (A, B, AB, O) possess the H antigen — Bombay group does not.

Genotype: hh — homozygous recessive for the H gene (FUT1 gene on chromosome 19).

Plasma contains anti-H (+ anti-A + anti-B) antibodies — cannot receive any other blood type.

Frequency: 1 in 10,000 in Mumbai; 1 in 1,000,000 in Europe.

On routine ABO typing, it appears as group O — but is genetically different.

In emergencies, Bombay group individuals can only receive blood from other Bombay donors.

What Is the Bombay Blood Group?

The Bombay blood group (hh phenotype / Oh group):

• First discovered: 1952, in Bombay (Mumbai), India • Discoverer: Dr. Y.M. Bhende (Indian haematologist) • Genotype: hh (homozygous recessive for the H gene) • H antigen: ABSENT from red blood cells (unlike all other ABO groups)

Normal ABO blood groups: • All ABO groups (A, B, AB, O) carry the H antigen • The H antigen is the base structure onto which A or B antigens are added • Group O: has H antigen but neither A nor B antigens

Bombay blood group: • Does NOT have the H antigen • Cannot form A or B antigens • Has anti-H antibodies in plasma (along with anti-A and anti-B) • On routine ABO typing, appears as blood group O — but is fundamentally different

Key distinction: Bombay group ≠ Blood group O Blood group O has H antigen (no A or B) Bombay group has NO H antigen at all

Genetics of Bombay Blood Group

Genetic basis: • The H antigen is coded by the H gene (FUT1 gene) on chromosome 19 • Normal allele: H (dominant) — produces H antigen • Bombay allele: h (recessive) — cannot produce H antigen

Genotypes: • HH or Hh: H antigen present → normal ABO group • hh: No H antigen → Bombay blood group

Since hh is homozygous recessive, both parents must carry at least one h allele for a child to have the Bombay phenotype.

Frequency: • India (Mumbai/Bombay region): 1 in 10,000 people • Western India: relatively more common • Europe/rest of world: 1 in 1,000,000 people • Overall: extremely rare globally

The higher frequency in Mumbai may be due to historical founder effect and consanguineous (related) marriages in certain communities.

Blood Transfusion and Medical Significance

Critical medical implications:

  1. Transfusion compatibility: • People with Bombay blood group can ONLY receive blood from other Bombay blood group donors • Cannot receive blood of any ABO group — even O negative — because all other blood has H antigen • Their plasma contains anti-H antibodies that attack H antigen on all other blood types → severe transfusion reaction (hemolysis)

  2. Blood transfusion crisis: • In medical emergencies, finding a compatible donor is extremely difficult • Bombay blood group individuals must pre-donate and store their own blood (autologous donation) • Blood banks in India (especially Mumbai) maintain a registry of Bombay blood group donors

  3. H antigen antibodies: • Anti-H antibodies in Bombay group are IgM class — very potent • Can cause life-threatening hemolytic transfusion reactions

  4. Inheritance: • Children of Bombay group parents may or may not have the phenotype depending on H gene status • If both parents are hh, all children will be Bombay group

Blood group registries: • Rare Donor Programme (ISBT) maintains a global list • In India, hospitals in Mumbai, Chennai, and Delhi maintain Bombay group donor registries

Questions and Answers

What is the Bombay blood group?+

The Bombay blood group (hh phenotype / Oh blood group) is an extremely rare blood type where the person lacks the H antigen on their red blood cells. It was first discovered in 1952 in Bombay (Mumbai) by Dr. Y.M. Bhende. People with this group cannot donate or receive blood from any standard ABO group.

Why is the Bombay blood group different from blood group O?+

Both Bombay blood group and group O have no A or B antigens on red blood cells. However, group O does have the H antigen. The Bombay blood group lacks even the H antigen (genotype hh). The Bombay group also has anti-H antibodies in plasma, which would cause severe reactions if H-antigen-carrying blood (all ABO groups including O) is transfused.

Who can donate blood to a person with Bombay blood group?+

Only another person with the Bombay blood group (hh phenotype) can donate blood to a Bombay blood group individual. All other blood types — including O negative — carry the H antigen, which triggers anti-H antibodies in the Bombay group person, causing a life-threatening hemolytic transfusion reaction.

What is the frequency of the Bombay blood group?+

The Bombay blood group occurs in about 1 in 10,000 people in the Mumbai (Bombay) region of India and is slightly more common in western India. In the rest of the world, it occurs in approximately 1 in 1,000,000 people — making it one of the rarest blood types globally.

What causes the Bombay blood group genetically?+

The Bombay blood group is caused by a homozygous recessive genotype (hh) for the H gene (FUT1 gene on chromosome 19). The H gene produces the H antigen. With two recessive copies (hh), no H antigen is produced. Since H antigen is needed to form A and B antigens, none of these are present either.

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