AMCD1

Introduction: AMCD1

Description of AMCD1

AMCD1 (medical condition): A form of arthrygryposis (congenital contractures) which tends to affect...more »

See also:

Arthrogryposis multiplex congenita, distal type 1:
  »Introduction: Arthrogryposis multiplex congenita, distal type 1
  »Symptoms of Arthrogryposis multiplex congenita, distal type 1

AMCD1: Rare Disease

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

AMCD1 is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that AMCD1, or a subtype of AMCD1, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

AMCD1 as a Disease

AMCD1: Another name for Arthrogryposis multiplex congenita, distal type 1 (or close medical condition association).
  »Introduction: Arthrogryposis multiplex congenita, distal type 1
  »Symptoms of Arthrogryposis multiplex congenita, distal type 1

AMCD1: Related Diseases

AMCD1: AMCD1 is listed as a type of (or associated with) the following medical conditions in our database:

• Joint conditions
• Musculoskeletal conditions
• Congenital conditions - physical defects
• Congenital conditions

Symptoms of AMCD1 (Arthrogryposis multiplex congenita, distal type 1)

Some of the symptoms of AMCD1 incude:

• Camptodactyly
• Clasp thumb
• Overlapping fingers
• Talipes varus
• Talipes valgus

See full list of 8 symptoms of AMCD1 (Arthrogryposis multiplex congenita, distal type 1)

Terms associated with AMCD1:

Terms Similar to AMCD1:

• DA 1
• Distal arthrogryposis, type 1
• Arthrogryposis multiplex congenita, distal type 1

Source - NIH

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