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MORM syndrome

Also Known As:

Mental Retardation, Truncal Obesity, Retinal Dystrophy, And Micropenis; Mental retardation, truncal Obesity, Retinal dystrophy and Micropenis

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

Disease Context: Research Results

Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Congenital Abnormalities: 25723
  - Multiple Abnormalities: 211
    - MORM syndrome: 1
Eye Diseases: 3522
- MORM syndrome: 1
Nervous System Diseases: 14178
- Neurologic Manifestations: 7102
  - Neurobehavioral Manifestations: 1586
    - Intellectual Disability: 8035
      - MORM syndrome: 1
Signs and Symptoms Pathological Conditions
- Signs and Symptoms
  - Body Weight: 130203
    - Overweight: 21719
      - Obesity: 108607
        MORM syndrome: 1
  - Neurologic Manifestations: 7102
    - Neurobehavioral Manifestations: 1586
      - Intellectual Disability: 8035
        MORM syndrome: 1
Behavior and Behavior Mechanisms
- Neurobehavioral Manifestations: 1586
  - Intellectual Disability: 8035
    - MORM syndrome: 1
Mental Disorders: 24177
- Neurodevelopmental Disorders: 3095
  - Intellectual Disability: 8035
    - MORM syndrome: 1
Nutritional and Metabolic Diseases: 15
- Nutrition Disorders: 404
  - Overnutrition: 616
    - Overweight: 21719
      - Obesity: 108607
        MORM syndrome: 1
Urogenital Diseases: 126
- Genital Diseases: 114
  - Male Genital Diseases: 2
    - Penile Diseases: 11
      - MORM syndrome: 1
- Male Urogenital Diseases
  - Male Genital Diseases: 2
    - Penile Diseases: 11
      - MORM syndrome: 1

Experts

1.	Ahmad, Wasim: 1 article (11/2019)
2.	Baple, Emma L: 1 article (11/2019)
3.	Crosby, Andrew H: 1 article (11/2019)
4.	Gul, Asma: 1 article (11/2019)
5.	Harlalka, Gaurav V: 1 article (11/2019)
6.	Hassan, Muhammad Jawad: 1 article (11/2019)
7.	Khalid, Sumbul: 1 article (11/2019)
8.	Khan, Shazia: 1 article (11/2019)
9.	Lin, Siying: 1 article (11/2019)
10.	Mehmood, Sarmad: 1 article (11/2019)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to MORM syndrome:

1.	Nonsense Codon (Nonsense Mutation)IBA 11/01/2019 - "Whole-exome sequencing identified the likely causes of disease as a novel homozygous frameshift mutation (NM_152384.2: c.196delA; p.(Arg66Glufs12); family 1) in BBS5, and a nonsense mutation (NM_019892.5:c.1879C>T; p.Gln627; family 2) in INPP5E, previously reported in an extended Pakistani family with MORM syndrome. "