Concept information
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Hereditary disease
Autosomal hereditary disorder
Recessive hereditary disorder, NOS
Autosomal recessive ichthyosis (disorder)
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Skin finding
Rough skin (finding)
Congenital ichthyosis of skin
Autosomal recessive ichthyosis (disorder)
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Lesion of skin and/or skin-associated mucous membrane
Skin lesion
Neoplasm of skin
Neuroectodermal dysplasia
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Lesion of skin and/or skin-associated mucous membrane
Mass of skin
Neoplasm of skin
Neuroectodermal dysplasia
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Finding of brain
Disease of brain
Congenital anomaly of brain
Congenital anomaly of cerebrum (disorder)
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Disease of the central nervous system
Disease of brain
Congenital anomaly of brain
Congenital anomaly of cerebrum (disorder)
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Disease of head
Disease of brain
Congenital anomaly of brain
Congenital anomaly of cerebrum (disorder)
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Disease of head
Disease of brain
Congenital anomaly of brain
Congenital anomaly of cerebrum (disorder)
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Disease of head
Congenital anomaly of head
Congenital anomaly of brain
Congenital anomaly of cerebrum (disorder)
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Disease of head
Congenital anomaly of head
Congenital anomaly of brain
Congenital anomaly of cerebrum (disorder)
Preferred term
Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome (disorder)
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Broader concept
Associated morphology
Finding site
- 181544004
- 181566006
- Entire skin
- nervous system
- skin
- Supratentorial brain
Has interpretation
Interprets
Is a
Occurrence
Pathological process
In other languages
URI
http://www.irandoc.acir/onto/irandoc/722385008
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