|
(HPO:0001249) | Intellectual disability | 1089 / 7739 | ||||
|
(HPO:0003108) | Hyperglycinuria | 11 / 7739 | ||||
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(OMIM) | Indolylacroyl glycinuria | 1 / 7739 | ||||
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(OMIM) | Transmucosal transport defect | 1 / 7739 | ||||
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(HPO:0000007) | Autosomal recessive inheritance | 2538 / 7739 |