UNIQUE – Rare Chromosome Disorder Support Group
About UNIQUE – Rare Chromosome Disorder Support Group
The UNIQUE – The Rare Chromosome Disorder Support Group is a non-profit, voluntary organization dedicated to promoting awareness of rare chromosomal abnormalities. The organization was founded in 1984 and served as a source of support and information for anyone affected by any rare chromosome abnormality. UNIQUE acts as an international support group; produces a newsletter for registered members; and promotes awareness of rare chromosomal abnormalities, both among the public and relevant professionals. It maintains a database holding the karyotypes, phenotypes and natural histories of all affected members.
Related Rare Diseases:
- MEF2C Deficiency
- ADNP Syndrome
- KAT6A Syndrome
- Dup15q Syndrome
- Phelan-McDermid Syndrome
- Cat Eye Syndrome
- Trisomy 9p (Multiple Variants)
- Mosaic Trisomy 9
- Trisomy X
- Chromosome 21 Ring
- Mosaic Trisomy 22
- Ring Chromosome 4
- Chromosome 15 Ring
- Chromosome 18q- Syndrome
- Chromosome 18 Ring
- Chromosome 14 Ring
- Chromosome 9 Ring
- Chromosome 22 Ring
- Chromosome 6 Ring
- XYY Syndrome
- Chromosome 4q Deletion
- Penta X Syndrome
- Triploidy
- Pallister Killian Mosaic Syndrome
- Trisomy 13 Syndrome
- Trisomy 18
- Cri du Chat Syndrome
- 48, XXYY Syndrome
- KAT6B-Related Disorders
- CTNNB1 Syndrome
- Síndrome CTNNB1
- ASXL3-Related Disorder
- Chromosome 9, Partial Monosomy 9p
- Síndrome de anomalías congénitas múltiples asociado al gen KAT6B
- Síndrome del ojo de gato
- Síndrome de Phelan-McDermid
- HNRNPU-Related Disorder
- Chromosome 11, Partial Monosomy 11q
- Trisomía 9 en mosaico
- Trastorno relacionado a HNRNPU
- Síndrome de Jacobsen (monosomía parcial 11q)
- Trisomía 22 en mosaico
- Síndrome KAT6A
- Síndrome 48,XXYY
- Trisomía 18
