HOME PRODUCTS COMPANY CONTACT FAQ

Research Dictionary Pharma

Sign Up FREE or Login

Microcephaly-Micromelia Syndrome

Networked: 1 relevant articles (0 outcomes, 0 trials/studies)

Disease Context: Research Results

Musculoskeletal Diseases: 719
- Bone Diseases: 5863
  - Developmental Bone Diseases: 153
    - Osteochondrodysplasias: 592
      - Microcephaly-Micromelia Syndrome: 1
- Musculoskeletal Abnormalities: 43
  - Craniofacial Abnormalities: 203
    - Microcephaly: 1471
      - Microcephaly-Micromelia Syndrome: 1
Nervous System Diseases: 14178
- Nervous System Malformations: 35
  - Malformations of Cortical Development: 376
    - Group I Malformations of Cortical Development
      - Microcephaly: 1471
        Microcephaly-Micromelia Syndrome: 1
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Musculoskeletal Abnormalities: 43
    - Craniofacial Abnormalities: 203
      - Microcephaly: 1471
        Microcephaly-Micromelia Syndrome: 1
  - Nervous System Malformations: 35
    - Malformations of Cortical Development: 376
      - Group I Malformations of Cortical Development
        Microcephaly: 1471
        Microcephaly-Micromelia Syndrome: 1
- Inborn Genetic Diseases: 11939
  - Osteochondrodysplasias: 592
    - Microcephaly-Micromelia Syndrome: 1

Experts

1.	Barkovich, A James: 1 article (01/2017)
2.	Blakley, Patricia: 1 article (01/2017)
3.	Chibbar, Rajni: 1 article (01/2017)
4.	Cordero, Dwight R: 1 article (01/2017)
5.	Coulter, Michael E: 1 article (01/2017)
6.	Diaz, Diana G: 1 article (01/2017)
7.	Diudea, Dana: 1 article (01/2017)
8.	Elhosary, Princess C: 1 article (01/2017)
9.	Evrony, Gilad D: 1 article (01/2017)
10.	Folkerth, Rebecca: 1 article (01/2017)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Microcephaly-Micromelia Syndrome:

1.	RNA (Ribonucleic Acid)IBA 01/01/2017 - "We report the integration of transcriptome sequencing (RNA-seq), which surveys all mRNAs to reveal functional impacts of variants at the transcription level, into the gene discovery framework for a unique human disease, microcephaly-micromelia syndrome (MMS). "