KID syndrome, autosomal recessive

Introduction: KID syndrome, autosomal recessive

Description of KID syndrome, autosomal recessive

KID syndrome, autosomal recessive (medical condition): A very rare recessively inherited disorder characterized by deafness, eye...more »

See also:

Ichthyosiform erythroderma, corneal involvement, deafness:
  »Introduction: Ichthyosiform erythroderma, corneal involvement, deafness
  »Symptoms of Ichthyosiform erythroderma, corneal involvement, deafness

KID syndrome, autosomal recessive: Related Topics

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

• KID syndrome
• Autosomal recessive
• Autosomal recessive disease
• Autosomal
• Autosomal diseases
• Recessive
• Recessive diseases

KID syndrome, autosomal recessive: Rare Disease

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

KID syndrome, autosomal recessive 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 recessive, or a subtype of KID syndrome, autosomal recessive, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

KID syndrome, autosomal recessive as a Disease

KID syndrome, autosomal recessive: Another name for Ichthyosiform erythroderma, corneal involvement, deafness (or close medical condition association).
  »Introduction: Ichthyosiform erythroderma, corneal involvement, deafness
  »Symptoms of Ichthyosiform erythroderma, corneal involvement, deafness

KID syndrome, autosomal recessive: Related Diseases

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

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

Symptoms of KID syndrome, autosomal recessive (Ichthyosiform erythroderma, corneal involvement, deafness)

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

• Red scaly skin patches
• Thickened patches of skin
• Sensorineural deafness
• Scarring alopecia
• Keratitis

See full list of 6 symptoms of KID syndrome, autosomal recessive (Ichthyosiform erythroderma, corneal involvement, deafness)

Terms associated with KID syndrome, autosomal recessive:

Terms Similar to KID syndrome, autosomal recessive:

• Keratitis-ichthyosis-deafness syndrome, autosomal recessive
• Ichthyosiform erythroderma, corneal involvement, deafness
• Desmons syndrome

Source - NIH

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