Phenotypes for disease #00776 (BFLS (Borjeson-Forssman-Lehmann syndrome (BFLS)), OMIM:301900)

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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     
0000298280 Global developmental delay, Motor delay, Hypotonia, Infantile muscular hypotonia, Strabismus, Hypoglycemia, Neonatal hypoglycemia, Esodeviation, Patent foramen ovale, Constipation, Atrial septal defect, Plagiocephaly, Abnormality of calvarial morphology, Abnormal corpus callosum morphology, Agenesis of corpus callosum, Aplasia/Hypoplasia of the corpus callosum, Sleep disturbance, Sleep apnea, Abnormal testis morphology, Retractile testis, Lacrimal duct stenosis, Nasolacrimal duct obstruction - - Familial, X-linked recessive 01y - - - - Andreas Laner 00405783
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