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(HPO:0000280) | Coarse facial features | Very frequent [Orphanet] | 189 / 7739 | |||
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(HPO:0000821) | Hypothyroidism | Very frequent [Orphanet] | 141 / 7739 | |||
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(HPO:0001252) | Muscular hypotonia | Very frequent [Orphanet] | 990 / 7739 | |||
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(HPO:0001324) | Muscle weakness | Very frequent [Orphanet] | 859 / 7739 | |||
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(HPO:0002019) | Constipation | Very frequent [Orphanet] | 194 / 7739 | |||
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(HPO:0002360) | Sleep disturbance | Very frequent [Orphanet] | 113 / 7739 | |||
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(HPO:0004322) | Short stature | Frequent [Orphanet] | 1232 / 7739 | |||
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(HPO:0010318) | Aplasia/Hypoplasia of the abdominal wall musculature | Very frequent [Orphanet] | 55 / 7739 | |||
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(HPO:0000158) | Macroglossia | Very frequent [Orphanet] | 119 / 7739 | |||
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(HPO:0005990) | Thyroid hypoplasia | Very frequent [Orphanet] | 21 / 7739 | |||
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(HPO:0000271) | Abnormality of the face | Very frequent [Orphanet] | 108 / 7739 | |||
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(HPO:0000239) | Large fontanelles | Very frequent [Orphanet] | 135 / 7739 | |||
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(HPO:0012758) | Neurodevelopmental delay | Frequent [Orphanet] | 949 / 7739 |