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Parietal foramina 2

MONDO:0012309

Any parietal foramina in which the cause of the disease is a mutation in the ALX4 gene.

Also known as: ALX4 parietal foramina, parietal foramina 2, parietal foramina caused by mutation in ALX4, parietal foramina type 2, PFM2

40 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Nervous system disorder (217) Musculoskeletal system disorder (196) Hereditary disease (172) Bone disorder (47) Human disease (14) Neural tube defect (11) Developmental defect during embryogenesis (7) Central nervous system malformation (5) Hereditary neurological disease (5)

Trials to join now! 20 Not yet recruiting 6 Not yet finished but already full! 4 Completed 9 Terminated 1

Scientists gather leftover surgical tissue to unlock secrets of bone disease

Knowledge-focused Terminated

This study collected bone, cartilage, skin, and fat tissue from 50 patients undergoing surgery at Children's National Medical Center. The goal was to grow cells from these tissues in the lab and analyze them to better understand bone and connective tissue diseases. The study was …

Sponsor: National Institute of Dental and Craniofacial Research (NIDCR) • Aim: Knowledge-focused

Last updated Jun 27, 2026 07:52 UTC