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Feingold syndrome type 2
rareFeingold syndrome type 2 (FS2) is a rare inherited malformation syndrome characterized by skeletal abnormalities and mild intellectual disabilities similar to those seen in Feingold syndrome type 1 (FS1) but that lacks the manifestations of gastrointestinal atresia and short palpebral fissures.
- Identifiers
- MONDO:0013691 OMIM:614326Orphanet:391646
- Causal genes
- MIR17HG
- Part of
- Feingold syndrome
- Also known as
- brachydactyly-short stature-microcephaly syndrome · Brunner-Winter syndrome type 2 · Feingold syndrome 2 · FGLDS2 · FS2
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