Gene |
Chromosome |
Location |
Syndrome |
Category |
ZBTB20 | 3 | q13.31 | Primrose syndrome | Autism spectrum | |
ZC4H2 | 23 | q11.2 | Wieacker-Wolf syndrome | Arthrogryposis spectrum | |
ZEB2 | 2 | q22.3 | Mowat-Wilson syndrome | Microcephaly | |
ZFAT | 8 | q24.22 | Thyroid disorders | Hypothyroidism | |
ZFP57 | 6 | p22.1 | 6q24-related transient neonatal diabetes mellitus | Diabetes | |
ZIC1 | 3 | q24 | ZIC FAMILY MEMBER 1 | Autism spectrum | |
ZIC2 | 13 | q32.3 | Microcephaly - other | Microcephaly | |
ZIC2 | 13 | q32 | Nonsyndromic holoprosencephaly | Cleft lip / cleft palate | |
ZIC3 | 23 | q26.3 | heterotaxy syndrome | Heterotaxy | |
ZIC4 | 3 | q24 | heterotaxy syndrome | Heterotaxy | |
ZMYND11 | 10 | p15.3 | ZINC FINGER MYND DOMAIN-CONTAINING PROTEIN 11 | Autism spectrum | |
ZNF335 | 20 | q13.12 | Microcephaly 10 primary autosomal recessive (MCPH10) | Microcephaly | |
ZNF407 | 18 | q22.3 | ZINC FINGER PROTEIN 407 | Autism spectrum | |
ZNF462 | 9 | q31.2 | Mental retardation autosomal dominant 40 | Autism spectrum | |
ZNF592 | 15 | q25.3 | Autosomal recessive spinocerebellar ataxia | Ataxia spectrum | |
ZNF713 | 7 | p11.2 | Zinc Fingers syndrome | Autism spectrum | |
ZNF717 | 3 | p12.3 | Autism 18 (AUTS18) | Autism spectrum | |
ZSWIM6 | 5 | q12.1 | ZINC FINGER SWIM DOMAIN-CONTAINING PROTEIN 6 | Autism spectrum | |
ZTTKS | 21 | q22.11 | ZTTK SYNDROME | Autism spectrum | |