Phenotypes for disease #03999 (SHFYNG (Schaaf-Yang syndrome (SHFYNG)), OMIM:615547)

11 entries on 1 page. Showing entries 1 - 11.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000060461 Schaaf-Yang syndrome (OMIM:615547) - - Isolated (sporadic) - - - - - Daniel Trujillano 00080892
0000129991 see paper; ... Prader-Willi syndrome-like SHFYNG Isolated (sporadic) 03y06m - - - - Yutak Negishi 00165096
0000129992 see paper; ... Prader-Willi syndrome-like SHFYNG Isolated (sporadic) 01y - - - - Yutak Negishi 00165097
0000129993 see paper; ... Prader-Willi syndrome-like SHFYNG Familial, autosomal dominant 12y - - - - Yutak Negishi 00165100
0000129995 see paper; ... Prader-Willi syndrome-like SHFYNG Familial, autosomal dominant 23y05m - - - - Yutak Negishi 00165099
0000129996 see paper; ... Prader-Willi syndrome-like SHFYNG Isolated (sporadic) 05y - - - - Yutak Negishi 00165095
0000130105 see paper; ... Prader-Willi syndrome-like SHFYNG Isolated (sporadic) 06y03m - - - - Yutak Negishi 00165098
0000351566 Intellectual disability, Obesity - - Unknown - - - - - Juliana Mazzeu 00466179
0000352572 see paper; ..., neonatal hypotonia, feeding difficulties, developmental delay, hypogonadismand distal contractures Schaaf-Yang syndrome SHFYNG Familial 01y02m - - - - Johan den Dunnen 00467365
0000352573 acc. Patak-31397880 arthrogryposis, hypomimia, high nasal bridge, micrognathia, bitemporal narrowing, high palate, prominent chin, low-set ears, epicanthic fold, club foot, respiratory distress, poor suck, open mouth, developmental delay, autism spectrum disorder, psychomotor delay, short stature Schaaf‐Yang syndrome SHFYNG Isolated (sporadic) 5y - - - - Johan den Dunnen 00467366
0000352574 acc. Patak-31397880 polyhydraominos, respiratory failure, apnea, hypotonia, tracheal stoma issues, poor suck, distal arthrogryposis, up-slanting palpebral fissures, bitemporal narrowing, high nasal bridge, low-set ears, prominent chin, micrognathia, developmental delay, autism spectrum disorder Schaaf‐Yang syndrome SHFYNG Isolated (sporadic) 9m - - - - Johan den Dunnen 00467367
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