Focal Dermal Hypoplasia

A genetic skin disease characterized by hypoplasia of the dermis, herniations of fat, and hand anomalies. It is found exclusively in females and transmitted as an X-linked dominant trait.

Also Known As:

Syndrome, Goltz; Goltz's Syndrome; Goltz-Gorlin Syndrome; Dermal Hypoplasias, Focal; Focal Dermal Hypoplasias; Goltzs Syndrome; Gorlin Syndrome, Goltz; Hypoplasia, Focal Dermal; Hypoplasias, Focal Dermal; Syndrome, Goltz Gorlin; Syndrome, Goltz's; Syndrome, Goltz-Gorlin; Dermal Hypoplasia, Focal; Goltz Gorlin Syndrome; Goltz Syndrome

Musculoskeletal Diseases: 719
- Bone Diseases: 5863
  - Developmental Bone Diseases: 153
    - Dysostoses: 91
      - Focal Dermal Hypoplasia: 29
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Multiple Abnormalities: 211
    - Ectodermal Dysplasia: 505
      - Focal Dermal Hypoplasia: 29
  - Skin Abnormalities: 159
    - Ectodermal Dysplasia: 505
      - Focal Dermal Hypoplasia: 29
- Inborn Genetic Diseases: 11939
  - Genetic Skin Diseases: 47
    - Ectodermal Dysplasia: 505
      - Focal Dermal Hypoplasia: 29
  - X-Linked Genetic Diseases: 42
    - Focal Dermal Hypoplasia: 29
Skin and Connective Tissue Diseases
- Skin Diseases: 13127
  - Skin Abnormalities: 159
    - Ectodermal Dysplasia: 505
      - Focal Dermal Hypoplasia: 29
  - Genetic Skin Diseases: 47
    - Ectodermal Dysplasia: 505
      - Focal Dermal Hypoplasia: 29

C R Darley Selected Research

C R Darley Research Topics

Disease

Drug/Important Bio-Agent (IBA)

Therapy/Procedure