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Chondrodysplasia punctate, rhizomelic, due to dihydroxyacetonephosphate acyl transferase deficiency (medical condition): A rare genetic disorder involving abnormal development...more »
See also:
Rhizomelic chondrodysplasia punctata, type 2:
»Introduction: Rhizomelic chondrodysplasia punctata, type 2
»Symptoms of Rhizomelic chondrodysplasia punctata, type 2
These medical condition or symptom topics may be relevant to medical information for Chondrodysplasia punctate, rhizomelic, due to dihydroxyacetonephosphate acyl transferase deficiency:
Chondrodysplasia punctate, rhizomelic, due to dihydroxyacetonephosphate acyl transferase deficiency: Another name for Rhizomelic chondrodysplasia punctata, type 2 (or close medical condition association).
»Introduction: Rhizomelic chondrodysplasia punctata, type 2
»Symptoms of Rhizomelic chondrodysplasia punctata, type 2
Chondrodysplasia punctate, rhizomelic, due to dihydroxyacetonephosphate acyl transferase deficiency: Chondrodysplasia punctate, rhizomelic, due to dihydroxyacetonephosphate acyl transferase deficiency is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Chondrodysplasia punctate, rhizomelic, due to dihydroxyacetonephosphate acyl transferase deficiency incude:
See full list of 9 symptoms of Chondrodysplasia punctate, rhizomelic, due to dihydroxyacetonephosphate acyl transferase deficiency (Rhizomelic chondrodysplasia punctata, type 2)
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