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Acromesomelic dysplasia, Grebe type (medical condition): A rare genetic disorder characterized by dwarfism and various...more »
See also:
Chondrodysplasia, Grebe type:
»Introduction: Chondrodysplasia, Grebe type
»Symptoms of Chondrodysplasia, Grebe type
These medical condition or symptom topics may be relevant to medical information for Acromesomelic dysplasia, Grebe type:
Acromesomelic dysplasia, Grebe type is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Acromesomelic dysplasia, Grebe type, or a subtype of Acromesomelic dysplasia, Grebe type,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when if affects 1 person per 2,000.
They list Acromesomelic dysplasia, Grebe type as a "rare disease".
Source - Orphanet
Acromesomelic dysplasia, Grebe type: Another name for Chondrodysplasia, Grebe type (or close medical condition association).
»Introduction: Chondrodysplasia, Grebe type
»Symptoms of Chondrodysplasia, Grebe type
Acromesomelic dysplasia, Grebe type: Acromesomelic dysplasia, Grebe type is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Acromesomelic dysplasia, Grebe type incude:
See full list of 9 symptoms of Acromesomelic dysplasia, Grebe type (Chondrodysplasia, Grebe type)
These medical disease topics may be related to Acromesomelic dysplasia, Grebe type:
Source: Diseases Database
Source - NIH
Source: Diseases Database
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