cyclopia sequence

A hereditary autosomal recessive form of holoprosencephaly which maps to chromosome 21. OMIM: 236100

Also Known As:

Cyclopia; Cyclopia defect; Demyer Sequence; Holoprosencephaly 1; cyclocephaly; cyclopian defect; synophthalmia

Musculoskeletal Diseases: 751
- Musculoskeletal Abnormalities: 46
  - Craniofacial Abnormalities: 208
    - Holoprosencephaly: 224
      - cyclopia sequence: 171
Nervous System Diseases: 14737
- Nervous System Malformations: 36
  - Agenesis of Corpus Callosum: 54
    - Holoprosencephaly: 224
      - cyclopia sequence: 171
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 960
- Congenital Abnormalities: 26404
  - Multiple Abnormalities: 213
    - Holoprosencephaly: 224
      - cyclopia sequence: 171
  - Chromosome Disorders: 140
    - Holoprosencephaly: 224
      - cyclopia sequence: 171
  - Musculoskeletal Abnormalities: 46
    - Craniofacial Abnormalities: 208
      - Holoprosencephaly: 224
        cyclopia sequence: 171
  - Nervous System Malformations: 36
    - Agenesis of Corpus Callosum: 54
      - Holoprosencephaly: 224
        cyclopia sequence: 171
- Inborn Genetic Diseases: 12342
  - Chromosome Disorders: 140
    - Holoprosencephaly: 224
      - cyclopia sequence: 171

Orsolya Roza Selected Research

Orsolya Roza Research Topics