ICD-11 classes
14 Diseases of the skin
Genetic and developmental disorders affecting the skin
ICD-11 Genetic and developmental disorders affecting the skin
A large group of disorders, some limited to the skin but many involving other organ systems, due to heritable genetic defects, chromosomal abnormalities or embryofetal developmental anomalies.
The diagnosis includes nothing.
The diagnosis excludes nothing.
Diagnosis contains 28 clarifying diagnoses:
- Genetic syndromes affecting the skin
It contains 5 clarifying diagnoses. - EC20 — Genetic disorders of keratinisation
It contains 7 clarifying diagnoses. - EC21 — Genetic defects of hair or hair growth
It contains 7 clarifying diagnoses. - EC22 — Genetic defects of nails or nail growth
It contains 2 clarifying diagnoses. - EC23 — Genetic disorders of skin pigmentation
It contains 4 clarifying diagnoses. - Genetically-determined epidermolysis bullosa
It contains 5 clarifying diagnoses. - Genetic disorders affecting dermal collagen, elastin or other matrix proteins
It contains 5 clarifying diagnoses. - Specified developmental anomalies affecting the skin
It contains 6 clarifying diagnoses. - Chromosomal disorders affecting the skin
It contains 8 clarifying diagnoses. - DNA instability syndromes affecting the skin
It contains 1 clarifying diagnosis. - Genetic disorders of adipose tissue or lipid metabolism affecting the skin
It contains 4 clarifying diagnoses. - Genetic disorders of amino acid metabolism or transport affecting the skin
It contains 8 clarifying diagnoses. - Sphingolipidoses with skin manifestations
It contains 1 clarifying diagnosis. - LD27.5 — Genetic hamartoneoplastic syndromes affecting the skin
It contains 4 clarifying diagnoses. - 5C58.13 — Variegate porphyria
- 5C56.30 — Mucopolysaccharidosis type 1
- 5C56.31 — Mucopolysaccharidosis type 2
- 5C56.33 — Mucopolysaccharidosis type 6
- 5C64.20 — Acrodermatitis enteropathica
- 4A60 — Monogenic autoinflammatory syndromes
It contains 5 clarifying diagnoses. - 1F23.14 — Chronic mucocutaneous candidosis
- Congenital anomalies of skin development
It contains 1 clarifying diagnosis. - Developmental hamartomata of the epidermis and epidermal appendages
It contains 4 clarifying diagnoses. - Developmental anomalies of skin pigmentation
It contains 3 clarifying diagnoses. - Hamartomata derived from dermal connective tissue
It contains 2 clarifying diagnoses. - Developmental defects of hair or nails
It contains 2 clarifying diagnoses. - Developmental anomalies of cutaneous vasculature
It contains 5 clarifying diagnoses. - EC7Y — Other specified genetic and developmental disorders affecting the skin
The diagnosis is included in 19 other classes.
- Chromosomal disorders affecting the skin
- DNA instability syndromes affecting the skin
- Genetic disorders of adipose tissue or lipid metabolism affecting the skin
- Genetic disorders of amino acid metabolism or transport affecting the skin
- Sphingolipidoses with skin manifestations
- Genetic hamartoneoplastic syndromes affecting the skin (LD27.5)
- Variegate porphyria (5C58.13)
- Mucopolysaccharidosis type 1 (5C56.30)
- Mucopolysaccharidosis type 2 (5C56.31)
- Mucopolysaccharidosis type 6 (5C56.33)
- Acrodermatitis enteropathica (5C64.20)
- Monogenic autoinflammatory syndromes (4A60)
- Chronic mucocutaneous candidosis (1F23.14)
- Congenital anomalies of skin development (LC60-LC60)
- Developmental hamartomata of the epidermis and epidermal appendages (LC00-LC0Y)
- Developmental anomalies of skin pigmentation (LC10-LC1Y)
- Hamartomata derived from dermal connective tissue (LC20-LC2Y)
- Developmental defects of hair or nails (LC30-LC31)
- Developmental anomalies of cutaneous vasculature (LC50-LC5Z)