ICD-11 classes
20 Developmental anomalies
Multiple developmental anomalies or syndromes
LD2D — Phakomatoses or hamartoneoplastic syndromes
ICD-11 LD2D — Phakomatoses or hamartoneoplastic syndromes
The diagnosis has no description.
The diagnosis includes nothing.
It excludes 8 items.
- Ataxia-telangiectasia (4A01.31)
- familial dysautonomia [Riley-Day] (8C21.1)
- Rendu-Osler-Weber disease (LA90.00)
- Proteus syndrome (LD2C)
- Sturge-Weber syndrome (LD23)
- Enchondromatosis (2E83)
- Maffucci syndrome (LD2F.1)
- Angio-osteohypertrophic syndrome (LD26.60)
Diagnosis with code LD2D contains 7 clarifying diagnoses:
- LD2D.0 — Peutz-Jeghers syndrome
- LD2D.1 — Neurofibromatoses
It contains 5 clarifying diagnoses. - LD2D.2 — Tuberous sclerosis
- LD2D.3 — Gardner syndrome
- LD2D.4 — Gorlin syndrome
- LD2D.Y — Other specified phakomatoses or hamartoneoplastic syndromes
- LD2D.Z — Phakomatoses or hamartoneoplastic syndromes, unspecified
The diagnosis is included in 9 other classes.
- NAME syndrome (2F01)
- Von Hippel-Lindau disease (5A75)
- Focal dermal hypoplasia (LD27.0Y)
- Epidermal naevus syndrome (LC02)
- Lumbosacral dermal melanocytosis (LC10)
- Naevus of Ota (LC10)
- Naevus of Ito (LC10)
- Dermal melanocyte hamartoma (LC10)
- Hereditary leiomyomatosis and renal cell cancer (2C90.Y)