Synonyms: Brachydactyly-short stature-microcephaly syndrome | Brunner-Winter syndrome type 2 | FGLDS2 | FS2 | MMT type 2 | Microcephaly-digital anomalies-normal intelligence syndrome type 2 | Microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 2
A rare genetic congenital malformation syndrome characterized by microcephaly short stature digital anomalies (brachymesophalangy fifth finger clinodactyly syndactyly of toes and hypoplastic thumbs) and mild intellectual disabilities but that lacks the manifestations of gastrointestinal atresia.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2026
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Feingold syndrome type 2?
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Advocacy Organizations
PPP2CA Pathways
PPP2CA Pathways connects families, shares strength, and supports the research community in the search for answers to Houge-Janssens Syndrome type 3.
Wave of Support, Inc
Empowering those affected by bleeding disorders and other rare disease through advocacy, resources, education, and support
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Clinical Trials
For a list of clinical trials in this disease area, please click here.