syndromic disease multiple congenital anomalies/dysmorphic syndrome-intellectual disability ataxia-photosensitivity-short stature syndrome https://github.com/monarch-initiative/mondo/issues/7181 https://rarediseases.info.nih.gov/diseases/2287/fenton-wilkinson-toselano-syndrome https://www.malacards.org/card/ataxia_photosensitivity_short_stature_syndrome A rare, genetic, multiple congenital anomalies/dysmorphic syndrome characterized by cerebellar-like ataxia, photosensitivity (mainly of the face and trunk), short stature and intellectual disability. Additional features include clinodactyly, single palmar transverse crease, high-arched palate, pseudohypertrophy of the calves and aortic valve lesions. There have been no further descriptions in the literature since 1983. Fenton Wilkinson Toselano syndrome GARD:0002287 UMLS:C4751230 MONDO:0015248 Orphanet:1184 Fenton-Wilkinson-Toselano syndrome MEDGEN:1655873 hereditary ataxia