Arthrogryposis multiplex congenita, distal, type 2A

Introduction: Arthrogryposis multiplex congenita, distal, type 2A

Description of Arthrogryposis multiplex congenita, distal, type 2A

Arthrogryposis multiplex congenita, distal, type 2A (medical condition): A genetic musculoskeletal disorder characterized mainly by...more »

See also:

Gordon Syndrome:
  »Introduction: Gordon Syndrome
  »Symptoms of Gordon Syndrome

Arthrogryposis multiplex congenita, distal, type 2A: Related Topics

These medical condition or symptom topics may be relevant to medical information for Arthrogryposis multiplex congenita, distal, type 2A:

• Arthrogryposis multiplex congenita, distal
• Arthrogryposis multiplex congenita
• Arthrogryposis (47 causes)
• Distal
• Type

Arthrogryposis multiplex congenita, distal, type 2A: Rare Disease

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

Arthrogryposis multiplex congenita, distal, type 2A is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Arthrogryposis multiplex congenita, distal, type 2A, or a subtype of Arthrogryposis multiplex congenita, distal, type 2A, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Arthrogryposis multiplex congenita, distal, type 2A as a Disease

Arthrogryposis multiplex congenita, distal, type 2A: Another name for Gordon Syndrome (or close medical condition association).
  »Introduction: Gordon Syndrome
  »Symptoms of Gordon Syndrome

Arthrogryposis multiplex congenita, distal, type 2A: Related Diseases

Arthrogryposis multiplex congenita, distal, type 2A: Arthrogryposis multiplex congenita, distal, type 2A is listed as a type of (or associated with) the following medical conditions in our database:

• Genetic conditions
• Hand conditions
• Foot conditions
• Limb conditions
• Congenital conditions - physical defects
• Congenital conditions
• Bone or skeletal conditions
• Musculoskeletal conditions
• Head conditions

Symptoms of Arthrogryposis multiplex congenita, distal, type 2A (Gordon Syndrome)

Some of the symptoms of Arthrogryposis multiplex congenita, distal, type 2A incude:

• Camptodactyly
• Cleft palate
• Club foot
• Fingerprint abnormalities
• Impaired mobility of lower arm joints

See full list of 12 symptoms of Arthrogryposis multiplex congenita, distal, type 2A (Gordon Syndrome)

Arthrogryposis multiplex congenita, distal, type 2A: Related Disease Topics

These medical disease topics may be related to Arthrogryposis multiplex congenita, distal, type 2A:

• rrae tubeular defect
• short stature
• weakness
• intellectual impairment
• autosomal dominant inheritance
• dental abnormalities
• sever hypertension
• chloride channel mutation
• renal tubular defect
• muscle weakness
• impaired growth during childhood
• severe hypertension

Terms associated with Arthrogryposis multiplex congenita, distal, type 2A:

Terms Similar to Arthrogryposis multiplex congenita, distal, type 2A:

• Camptodactyly, cleft palate and clubfoot
• DA3
• Distal arthrogryposis, type 3
• Gordon syndrome

Source - NIH

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2,3-diketo-l-gulonate

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