# data[].attributes.body
1:    it can change the white in your eyes to blue,purple,or gray tints in the eye.
2:     the done is very weak so it can break at little to know cause at all.
3: this mutation is one that can have 6 different stages of how bad this decease.

# data[].attributes.body
1. infants loss motor skill like turning over, sitting and crawling
2. as the disease progresses they start losing vision and hearing
3. sometimes only live to there early childhood

# data[].attributes.body
1. Noonan Syndrome is a disorder that involves unusual facial characteristics.
2. some symptoms are short stature, heart defects at birth, bleeding problem and much more.
3. cures for Noonan Syndrome are growth hormone treatment.
The heart defects can't be fixed, or cured.

# data[].attributes.body
1.May cause result in lung disease or liver disease
2.May result in shortness of breath, wheezing, or an increased risk of lung infection
3. Outset of Lung problems is typically between 20 and 50 years old

# data[].attributes.body
1.A common birth defect of the brain.

2.Can cause cleft lips, small head size, and other birth defects.

3. In the most severe cases
holoprosencephaly can cause cyclopia, when a single eye is located where the bridge of the nose would be.

# data[].attributes.body
1. A rare muscle mutation appeared only in boys.

2.Weakenss your muscles so that you cans walk or move your arms.

3. At a young age you cant even see the any symptoms, The older you get the more easier it is to see the symptoms

# data[].attributes.body
1. Some Symptoms:
- Heart attacks of fever
- Inflammation of the abdominal lining (peritonitis)
- Inflammation of the lining surrounding the lungs (pleurisy)
- Painfully swollen joints (arthralgia  and occasionally arthritis  )
- Ankle rash
2. Is considered a rare disease world wide, however is very common in people of Sephardi. (Jewish, Armenian, Arab, and Turkish.)
- About 1 in 200 people have Familial Mediterranean Fever.
3. Familial Mediterranean Fever disease is a recessive inherited disease. It only appears in people who received two copies it the mutation a gene that causes FMF , one from each parent.

# data[].attributes.body
1. symptoms: hand and arm abnormalities make the disorder more apparent early in life
2. Treated by: some treatments is reconstructive surgery on the muscles

# data[].attributes.body
1. Cause is unknown
2. Swelling in the bowel is very painful and causes diarrhea, abnormal pain, nausea and decreased appetite
3. Crohn's Disease is usually diagnosed to people at the age of 20 - 30, and about 25% of people with Crohn's Disease are under the age of 20.

# data[].attributes.body
1.  Resessive
2.   Affects about 1 in 10,000 Americans.
3. Makes it harder to breath or swallow

# data[].attributes.body
1.No speech or minimal speech. Difficulty walking, moving or balancing
2. Sedative can help with the disorder it helps calm you down and therapy.
3. symptoms of this disorder are problems with movement and balance, small head size, flatness in the back of the head, and frequent laughter.

# data[].attributes.body
1. symptoms are decreased or poor muscle tone, short neck with excess skin at the back of the neck flattened facial profile and nose, small head ears and mouth, white spots on the colored part of the eyes, wide or short hands with short fingers, a single deep crease across the palm of the hand, also deep groove between the first and second toes. Causes of Down Syndrome are caused by an error in cell division called nondisjunction that leaves a sperm or egg cell with an extra copy of chromosome 21 before or at conception. 3. there is no cure but there is treatment.

# data[].attributes.body
1. symptoms:
TREMORS : can occur when resting, in hands or limbs.
Shaking all of the time.

# data[].attributes.body
1. A  rare  eye movement disorder
2. There is no cure for Duane Syndrome
3.  80% of the people with DS have  only one eye affected, most often the left
4. 1-5% of people are affected by Duane Syndrome.

# data[].attributes.body
1. Causes increased aging

2. Affects 4 million newborns worldwide

3.Children with progeria usually die at the age of 13

4. Symptoms include:
slow hair growth and hair loss.

# data[].attributes.body
1. Symptoms:

Jaundice

Fatigue

Loss of appetite

Swelling in the abdomen

Easy bruising

2. Treated by:

Removing the excess copper from the body.

Reducing intake of foods that are rich in copper.

Treating any liver or central nervous system damage.

3. Inherited by: In this pattern of inheritance, a person needs to inherit two altered (mutated) copies of a gene - one from each parent - to develop the disease.

# data[].attributes.body
1. 40-100 people are diagnosed with SCID in the United States.
2. The most effective treatment for SCID is a bone marrow transplant.
3. SCID is caused by several possible genes and makes you highly susceptible to life threatening infections by viruses.

# data[].attributes.body
1. Fingers are toes are fused together.
2. Affects from the skull growing normally.
3. The head is big and fingers and toes are stick together.

# data[].attributes.body
1.Disease can last for years or lifetime
2. No cure
3. Affects all kinds of races.

# data[].attributes.body
1.it´s is a blood clot
2.it is a missing or defected factor
3 affected all kind of races

# data[].attributes.body
1.) caused by having only 1 X chromosomes humans normally have 2
2.) Some symptoms are delayed puberty, abnormality's in reproductive organs ,kidney malformation, and a lot more.
3.) 98% of babies with turner syndrome die.

# data[].attributes.body
1. Recessive genetic disease                 2.their are approximately 30,000 in the united states that are affected with cystic fibrosis 3. affects all kinds of races

# data[].attributes.body
1. Treatment: no treatment
2. it affects about 1 in 4000 males and 1 in 800 females

3: There is currently no cure

# data[].attributes.body
1. Phenotype: dwarfism
2. People who are affected usually have normal sized parents.
3. Intelligence and lifespan are normal for those affected.