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| created at |
2024-09-19 07:43:07 UTC |
| updated at |
2024-09-23 18:19:38 UTC |
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MedGen CUI
Namespace: https://www.ncbi.nlm.nih.gov/medgen/
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622,528 entries
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There is 0 pattern entry.
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AOS1
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C4551482 |
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Adams-Oliver syndrome
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C4551482 |
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Forrest H Adams syndrome
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C4551482 |
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ADAMS-OLIVER SYNDROME 1
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C4551482 |
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Adams-Oliver syndrome 1
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C4551482 |
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Familial aplasia cutis congenita of the scalp
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C4551482 |
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Aplasia cutis congenita with terminal transverse defects of limbs, and skull defects
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C4551482 |
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aplasia cutis congenita with terminal transverse limb defects
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C4551482 |
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aplasia cutis congenita, congenital heart defect, and frontonasal cysts
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C4551482 |
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Aplasia Cutis Congenita With Terminal Transverse Limb Defects
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C4551482 |
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Congenital Scalp Defects With Distal Limb Reduction Anomalies
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C4551482 |
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Adams-Oliver syndrome caused by mutation in ARHGAP31
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C4551482 |
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APLASIA CUTIS CONGENITA WITH TERMINAL TRANSVERSE LIMB DEFECTS
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C4551482 |
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CONGENITAL SCALP DEFECTS WITH DISTAL LIMB REDUCTION ANOMALIES
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C4551482 |
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ABSENCE DEFECT OF LIMBS, SCALP, AND SKULL
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C4551482 |
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