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(HPO:0002084) | Encephalocele | Frequent [Orphanet] | 70 / 7739 | |||
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(HPO:0001006) | Hypotrichosis | Frequent [Orphanet] | 219 / 7739 | |||
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(HPO:0001162) | Postaxial hand polydactyly | Very frequent [Orphanet] | 119 / 7739 | |||
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(HPO:0001362) | Calvarial skull defect | Frequent [Orphanet] | 22 / 7739 | |||
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(HPO:0005696) | Postaxial polydactyly type A | 1 / 7739 | ||||
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(HPO:0007385) | Aplasia cutis congenita of scalp | 10 / 7739 | ||||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 |