Concept information
Preferred term
Hereditary disorder of the integument
Type
-
http://www.irandoc.ac.ir/onto/irandoc-meta/Concept
Narrower concepts
- Curry-Hall syndrome
- Epidermolysis bullosa
- Familial chilblain lupus erythematosus (disorder)
- Familial cold urticaria
- Familial lichen amyloidosis
- Familial multiple trichodiscoma
- FAMMM - Familial atypical mole malignant melanoma syndrome
- Ferguson-Smith tumor
- Follicular atrophoderma and basal cell epitheliomata
- Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder)
- Hereditary palmoplantar keratoderma
- Hereditary striate leuconychia
- Hippocratic fingers
- Hypodontia and nail dysgenesis
- Inherited cutis laxa
- Inherited disorder of keratinization
- Kohlschutter's syndrome
- Mandibuloacral dysostosis
- Multiple fibrofolliculomas
- Multiple lentigines syndrome
- OFD IV - Orofacial-digital syndrome IV
- Orofacial-digital syndrome III
- PARC syndrome
- Poikilodermal cutaneous amyloid
- Tuberous sclerosis syndrome
- Weary-Kindler syndrome
Finding site
Is a
- 128598002
- 363137000
In other languages
-
Persian
URI
http://www.irandoc.acir/onto/irandoc/363185004
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