Phenotypes for disease #00013 (SPD (dwarfism, primordial, syndromic (SPD)))

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Diagnosis/Initial     

Inheritance     

Age/Examination     

Diagnosis/Definite     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Phenotype details     

Protein     

Owner     

Individual ID     
0000000013 - Unknown - - - - - - - Anas M Alazami 00000145
0000002027 - Isolated (sporadic) - - - - - lissencephaly, ambiguous genitalia, agenesis corpus callosum - Johan den Dunnen 00003187
0000002099 - Isolated (sporadic) - - - - - - - Johan den Dunnen 00003260
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