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Browse result for Delpire-McNeill syndrome
※ introduction Delpire-McNeill syndrome (DELMNES) is a neurodevelopmental disorder with highly variable manifestations. Patients present in infancy with global developmental delay, including motor, speech, and impaired intellectual development. The most severely affected patients have hypotonia, inability to hold their head or walk, bilateral sensorineural deafness, and absent language, whereas others have delayed walking and mild to moderate intellectual disability, often with speech delay and autistic features. More variable features may include spasticity or minor involvement of other organ systems, such as hip dislocation or ventricular septal defect.
Reference
OMIM: Delpire-McNeill syndrome
Reference
OMIM: Delpire-McNeill syndrome
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD05605 | P55011 | 6558 | SLC12A2 | Solute carrier family 12 member 2 -chloride cotransporter 2) | Homo sapiens |
