macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome
macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome
Explore linked clinical trials. Standard reference: MONDO:00147161 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| RASopathy Biorepository | Abnormalities, Multiple, Cardiovascular Abnormalities, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Costello syndrome, Craniofacial Abnormalities, Hyperpigmentation, Legius syndrome, Melanosis, Musculoskeletal Abnormalities, Neoplasms by Histologic Type, Neoplasms, Nerve Tissue, Noonan syndrome, Noonan syndrome with multiple lentigines, Skin and Connective Tissue Diseases, cardiofaciocutaneous syndrome, cardiovascular disorder, congenital heart disease, connective tissue disorder, heart disorder, heart valve disorder, hereditary disease, hereditary neoplastic syndrome, inherited neurodegenerative disorder, lentigo, macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome, musculoskeletal system disorder, neoplasm, nerve sheath neoplasm, nervous system disorder, neurocutaneous syndrome, neurodegenerative disease, neurofibroma, neurofibromatosis, neurofibromatosis type 1, neurofibromatosis-Noonan syndrome, neuromuscular disease, peripheral nervous system disorder, pulmonary valve stenosis, skin disorder, skin pigmentation disorder | Recruiting | Not stated | 2025-12-18 | NCT04395495 |