ACS5

Introduction: ACS5

Description of ACS5

ACS5 (medical condition): A rare genetic disorder where some of the skull bones...more »

See also:

Pfeiffer syndrome:
  »Introduction: Pfeiffer syndrome
  »Symptoms of Pfeiffer syndrome

ACS5: Rare Disease

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

ACS5 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that ACS5, or a subtype of ACS5, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

ACS5 as a Disease

ACS5: Another name for Pfeiffer syndrome (or close medical condition association).
  »Introduction: Pfeiffer syndrome
  »Symptoms of Pfeiffer syndrome

ACS5: Related Diseases

ACS5: ACS5 is listed as a type of (or associated with) the following medical conditions in our database:

• Heritable Disorders of Connective Tissue
• Head conditions
• Bone or skeletal conditions
• Musculoskeletal conditions
• Genetic conditions
• Congenital conditions - physical defects
• Nervous system conditions
• Hand conditions
• Foot conditions
• Limb conditions

Symptoms of ACS5 (Pfeiffer syndrome)

Some of the symptoms of ACS5 incude:

• Premature skull bone fusion
• Broad thumbs
• Broad toes
• Short thumbs
• Short toes

See full list of 16 symptoms of ACS5 (Pfeiffer syndrome)

ACS5: Related Disease Topics

These medical disease topics may be related to ACS5:

• genetic disorder
• type 1 pfeffer syndrome
• type 2 pfeiffer syndrome
• type 3 pfeiffer syndrome
• craniosynostosis

Terms associated with ACS5:

Terms Similar to ACS5:

• Acrocephalosyndactyly, type 5
• Pfeiffer type acrocephalosyndactyly
• Pfeiffer syndrome

Source - NIH

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