Phenotypes for disease #02070 (SHORT (SHORT syndrome (SHORT)), OMIM:269880)

6 entries on 1 page. Showing entries 1 - 6.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

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Owner     

Individual ID     
0000034687 see paper; SHORT syndrome, high IGFI levels, CNS defects, developmental delay, pronounced progeroid appearance, ... - - Familial, autosomal recessive - - - - - B. Augello 00046337
0000061388 - - - Unknown - - - - - Jelena Čalyševa 00079886
0000061389 - - - Unknown - - - - - Jelena Čalyševa 00079888
0000061390 - - - Unknown - - - - - Jelena Čalyševa 00079890
0000061391 - - - Unknown - - - - - Jelena Čalyševa 00079891
0000318902 see paper; ..., short stature, ocular depression, Rieger anomaly, teething delay; facial hirsutism, blue sclera, small upslanting palpebral fissures, hypoplastic alae nasi, full cheeks, thin upper lips, large dysplastic ears, micrognathia SHORT syndrome SHORT Isolated (sporadic) 23y - - - - Johan den Dunnen 00319854
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