hypotonia-cystinuria syndrome

Summary
Synonym
  • cystinuria with mitochondrial disease
Definition
A syndrome that has_material_basis_in homozygous deletion on chromosome 2p21 that disrupts the SLC3A1 and PREPL genes. The deletion ranges in size from 23.8 to 75.5 kb. Itis characterized_by neonatal and infantile hypotonia and failure to thrive, cystinuria type 1 and nephrolithiasis, growth retardation due to growth hormone deficiency, and minor facial dysmorphism.
Super Class
chromosomal deletion syndrome syndrome
External Links
Disease Ontology
DOID:0060858
Mondo Disease Ontology
MeSH
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6519 SLC3A1 solute carrier family 3 member 1
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q07837 Amino acid transporter heavy chain SLC3A1
The Human Phenotype Ontology
Displaying entries 11 - 20 of 25 in total
HPO ID HPO Term
HP:0002591 Polyphagia
HP:0001250 Seizure
HP:0003131 Cystinuria
HP:0001508 Failure to thrive
HP:0000508 Ptosis
HP:0001943 Hypoglycemia
HP:0000135 Hypogonadism
HP:0000278 Retrognathia
HP:0002901 Hypocalcemia
HP:0005280 Depressed nasal bridge
Displaying 1 entry
Gene ID Gene Symbol Description
6519 SLC3A1 solute carrier family 3 member 1

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Last updated: August 19, 2024