Chondrodystrophia calcificans congenita

Introduction: Chondrodystrophia calcificans congenita

Description of Chondrodystrophia calcificans congenita

Chondrodystrophia calcificans congenita (medical condition): A rare genetic disorder characterized by growth deficiency, short limbs,...more »

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Chondrodystrophia calcificans congenita:
  »Introduction: Chondrodystrophia calcificans congenita
  »Symptoms of Chondrodystrophia calcificans congenita

Chondrodystrophia calcificans congenita: Rare Disease

Ophanet

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

Source - Orphanet

Chondrodystrophia calcificans congenita as a Disease

Chondrodystrophia calcificans congenita (medical condition): See Chondrodystrophia calcificans congenita (disease information).
  »Introduction: Chondrodystrophia calcificans congenita
  »Symptoms of Chondrodystrophia calcificans congenita

Chondrodystrophia calcificans congenita: Related Diseases

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

• Genetic conditions
• Growth conditions
• Limb conditions
• Skin conditions
• Hair conditions
• Congenital conditions

More information on medical condition: Chondrodystrophia calcificans congenita:

• Information about Chondrodystrophia calcificans congenita
• Basic Summary for Chondrodystrophia calcificans congenita
• Symptoms of Chondrodystrophia calcificans congenita
• Complications of Chondrodystrophia calcificans congenita

Terms associated with Chondrodystrophia calcificans congenita:

Terms Similar to Chondrodystrophia calcificans congenita:

• Conradi-Huenermann syndrome
• Chondrodysplasia punctata, autosomal dominant
• Chondrodysplasia punctata, Conradi-Hunermann type

Source: Diseases Database

External links related to: Chondrodystrophia calcificans congenita

• OMIM - CHONDRODYSPLASIA PUNCTATA, AUTOSOMAL DOMINANT

Source: Diseases Database

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