- Decreased body weight (HP:0004325): Abnormally low body weight. Evidence: PCS. Frequency: 3/4. (PMID:28796236)
- Birth length less than 3rd percentile (HP:0003561). Evidence: PCS. Frequency: 5/5. Onset: Congenital onset (HP:0003577). (PMID:28796236)
- Small for gestational age (HP:0001518): Smaller than normal size according to sex and gestational age related norms, defined as a weight below the 10th percentile for the gestational age. Evidence: PCS. Frequency: 4/5. Onset: Congenital onset (HP:0003577). (PMID:28796236)
- Prominent forehead (HP:0011220): Forward prominence of the entire forehead, due to protrusion of the frontal bone. Evidence: PCS. Frequency: 4/5. (PMID:28796236)
- Feeding difficulties in infancy (HP:0008872): Impaired feeding performance of an infant as manifested by difficulties such as weak and ineffective sucking, brief bursts of sucking, and falling asleep during sucking. There may be difficulties with chewing or maintaining attention. Evidence: PCS. Frequency: 4/4. Onset: Infantile onset (HP:0003593). (PMID:28796236)
- Autosomal dominant inheritance (HP:0000006): A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele. Evidence: PCS. (PMID:28796236)
- Triangular face (HP:0000325): Facial contour, as viewed from the front, triangular in shape, with breadth at the temples and tapering to a narrow chin. Evidence: PCS. Frequency: 5/5. (PMID:28796236)
These phenotypes are associated with the disease silver-russell syndrome 4 (OMIM:618907).