KID syndrome, autosomal dominant

Introduction: KID syndrome, autosomal dominant

Description of KID syndrome, autosomal dominant

KID syndrome, autosomal dominant (medical condition): A rare genetic ectodermal disorder characterized by...more »

See also:

Senter syndrome:
  »Introduction: Senter syndrome
  »Symptoms of Senter syndrome
  »Causes of Senter syndrome

KID syndrome, autosomal dominant: Related Topics

These medical condition or symptom topics may be relevant to medical information for KID syndrome, autosomal dominant:

• KID syndrome
• Autosomal dominant
• Autosomal dominant disease
• Autosomal dominant disorder
• Autosomal
• Autosomal diseases
• Dominant
• Dominant diseases

KID syndrome, autosomal dominant: Rare Disease

Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

KID syndrome, autosomal dominant is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that KID syndrome, autosomal dominant, or a subtype of KID syndrome, autosomal dominant, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

KID syndrome, autosomal dominant as a Disease

KID syndrome, autosomal dominant: Another name for Senter syndrome (or close medical condition association).
  »Introduction: Senter syndrome
  »Symptoms of Senter syndrome
  »Causes of Senter syndrome

KID syndrome, autosomal dominant: Related Diseases

KID syndrome, autosomal dominant: KID syndrome, autosomal dominant is listed as a type of (or associated with) the following medical conditions in our database:

• Genetic conditions
• Skin conditions
• Ear and hearing conditions
• Head conditions
• Eye and vision conditions

Causes of KID syndrome, autosomal dominant

Some of the causes of KID syndrome, autosomal dominant are included in the list below:

• The condition is inherited in an autosomal dominant manner

Read more about causes of KID syndrome, autosomal dominant (Senter syndrome)

Symptoms of KID syndrome, autosomal dominant (Senter syndrome)

Some of the symptoms of KID syndrome, autosomal dominant incude:

• Sensorineural deafness
• Ichthyosiform erythroderma
• Lamellar ichthyosis
• Hyperkeratosis
• Ichthyosiform erythroderma on skin of palms

See full list of 37 symptoms of KID syndrome, autosomal dominant (Senter syndrome)

KID syndrome, autosomal dominant: Related Disease Topics

These medical disease topics may be related to KID syndrome, autosomal dominant:

• keratitis
• hepatitis
• icthyosis
• deafness
• sensorineural deafness
• neuromuscular disease
• cirrhosis

Terms associated with KID syndrome, autosomal dominant:

Terms Similar to KID syndrome, autosomal dominant:

• Senter syndrome
• Keratitis-ichthyosis-deafness syndrome, autosomal dominant

Source: Diseases Database

• Keratitis, Ichthyosis, and Deafness (KID) Syndrome
• Keratitis-ichthyosis-deafness syndrome, autosomal dominant
• KID syndrome

Source - NIH

External links related to: KID syndrome, autosomal dominant

• Search Jablonski's Syndromes Database
• OMIM - KERATITIS-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL DOMINANT

Source: Diseases Database

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Medical dictionaries:

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• Medical Acronymns/Abbreviations

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