eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | cleft palate |
| Comorbidity | C0010308|congenital hypothyroidism |
| Sentences | 2 |
| PubMedID- 20484477 | Context: homozygous loss-of-function mutations in forkhead box e1/thyroid transcription factor 2 (foxe1/ttf-2) cause syndromic congenital hypothyroidism, with thyroid dysgenesis, cleft palate, spiky hair, and variable choanal atresia and bifid epiglottis in three cases reported hitherto. |
| PubMedID- 24341142 | Bamforth syndrome is a rare inherited condition whose main features are congenital hypothyroidism due to thyroid dysplasia, cleft palate, and spiky hair, with or without choanal atresia and bifid epiglottis. |
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