Phenotypes for disease #01768 (SHFM6 (split-hand/foot malformation, type 6 (SHFM-6)), OMIM:225300)

6 entries on 1 page. Showing entries 1 - 6.
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     
0000059586 Affected individuals in this large consanguineous family showed variable prototypes of split hand foot malformation - - Familial, autosomal recessive - - - - - Irfan Ullah 00079873
0000173485 split hand, split foot, syndactyly split-hand/foot malformation split-hand/foot malformation Familial, autosomal recessive - - - - - Kaori Yamoto 00231002
0000173486 split hand, syndactyly split-hand/foot malformation split-hand/foot malformation Isolated (sporadic) - - - - - Kaori Yamoto 00231003
0000173487 split foot, polydactyly, Microphthalmia, cryptorchidism, global developmental delay split-hand/foot malformation split-hand/foot malformation Isolated (sporadic) - - - - - Kaori Yamoto 00231005
0000175568 split hand, syndactyly split-hand/foot malformation split-hand/foot malformation Familial - - - - - Kaori Yamoto 00235305
0000175606 split foot, ventricular septal defect split-hand/foot malformation split-hand/foot malformation Isolated (sporadic) - - - - - Kaori Yamoto 00231004
Legend   How to query  


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