Phenotypes for disease #00767 (GBBB1 (Opitz GBBB syndrome, type 1, X-linked (GBBB-1)), OMIM:300000)

3 entries on 1 page. Showing entries 1 - 3.
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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     
0000284835 Malformations of ventral midline suspected GBBB-1 - Familial, X-linked recessive - - - - - Lucia Micale 00391499
0000284836 Malformations of ventral midline suspected GBBB-1 GBBB-1 Unknown - - - - - Lucia Micale 00391500
0000284837 Malformations of ventral midline suspected GBBB-1 GBBB-1 Unknown - - - - - Lucia Micale 00391501
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