ABCD syndrome

Introduction: ABCD syndrome

Description of ABCD syndrome

ABCD syndrome (medical condition): A rare inherited condition characterized by albinism, deafness, a black...more »

See also:

ABCD syndrome:
  »Introduction: ABCD syndrome
  »Symptoms of ABCD syndrome

ABCD syndrome: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

ABCD syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that ABCD syndrome, or a subtype of ABCD syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Ophanet

Ophanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list ABCD syndrome as a "rare disease".

Source - Orphanet

ABCD syndrome as a Disease

ABCD syndrome (medical condition): See ABCD syndrome (disease information).
  »Introduction: ABCD syndrome
  »Symptoms of ABCD syndrome

ABCD syndrome: Related Diseases

ABCD syndrome: ABCD syndrome is listed as a type of (or associated with) the following medical conditions in our database:

• Genetic conditions
• Ear and hearing conditions
• Hair conditions
• Intestine conditions
• Digestive conditions
• Abdominal conditions
• Skin conditions
• Congenital conditions

More information on medical condition: ABCD syndrome:

• Information about ABCD syndrome
• Basic Summary for ABCD syndrome
• Symptoms of ABCD syndrome

ABCD syndrome: Related Disease Topics

These medical disease topics may be related to ABCD syndrome:

• albinism
• black lock
• cell migration disorder of the neurocytes of the gut
• sensorineural deafness
• Shah-waarenburg syndrome

Terms associated with ABCD syndrome:

Terms Similar to ABCD syndrome:

• Albinism, Black lock, Cell migration disorder of the neurocytes of the gut, and deafness

Source - NIH

External links related to: ABCD syndrome

• OMIM - ABCD SYNDROME

Source: Diseases Database

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