Phenotypes for disease #02878 (SCDO3 (dysostosis, spondylocostal, autosomal recessive, type 3 (SCDO-3)), OMIM:609813)

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000318904 Polyhydramnios HP:0001561 Respiratory distress HP:0002098 Kyphoscoliosis HP:0002751 Rib fusion HP:0000902 Hemivertebrae HP:0002937 Thoracic dysplasia HP:0006644 Pulmonary hypoplasia HP:0002089 Absent/hypoplastic coccyx HP:0008436 skeletal dysplasia Spondylocostal dysostosis 3 Familial, autosomal recessive 00y01m - - prenatal Beta-1,3-N-acetylglucosaminyltransferase lunatic fringe Edoardo Errichiello 00427959
0000318905 Respiratory distress HP:0002098 Hemivertebrae HP:0002937 Vertebral fusion HP:0002948 skeletal dysplasia Spondylocostal dysostosis 3 Familial, autosomal recessive - - - - Beta-1,3-N-acetylglucosaminyltransferase lunatic fringe Edoardo Errichiello 00427960
0000318906 Spinal dysraphism HP:0010301 Hemivertebrae HP:0002937 Rib fusion HP:0000902 Short stature HP:0004322 Pectus carinatum HP:0000768 Butterfly vertebrae HP:0003316 Pulmonary hypoplasia HP:0002089 skeletal dysplasia Spondylocostal dysostosis 3 Familial, autosomal recessive - - - - Beta-1,3-N-acetylglucosaminyltransferase lunatic fringe Edoardo Errichiello 00427961
0000321934 Short stature (10th to 25th %), vertebral segmental defects and rib fusions (9 right ribs and 10 left), left 38-degree scoliosis at L1/S1, 44-degree lordosis at L1/S1, and 32-degree kyphosis at T2/T12. - - Familial, autosomal recessive - - - - - Parker Cole Wengryn 00431334
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.