神经皮肤综合征 / Phakomatoses or hamartoneoplastic syndromes

http://purl.bmicc.cn/ontology/ICD11CN/LD2D

NAME syndrome (2F01)

Lumbosacral dermal melanocytosis (LC10)

Naevus of Ito (LC10)

Hereditary leiomyomatosis and renal cell cancer (2C90.Y)

Focal dermal hypoplasia (LD27.0Y)

Epidermal naevus syndrome (LC02)

Dermal melanocyte hamartoma (LC10)

Naevus of Ota (LC10)

Von Hippel-Lindau disease (5A75)

Rendu-Osler-Weber disease (LA90.00)

familial dysautonomia [Riley-Day] (8C21.1)

Sturge-Weber syndrome (LD23)

Proteus syndrome (LD2C)

Angio-osteohypertrophic syndrome (LD26.60)

Ataxia-telangiectasia (4A01.31)

Maffucci syndrome (LD2F.1)

Enchondromatosis (2E83)

http://id.who.int/icd/release/11/2019-04/mms/1427672516

神经皮肤综合征 / Phakomatoses or hamartoneoplastic syndromes

http://purl.bmicc.cn/ontology/ICD10CN/Q85

LD2D

ICD11CN:LD2D

神经皮肤综合征 / Phakomatoses or hamartoneoplastic syndromes

http://purl.bmicc.cn/ontology/ICD11CN/L1-LD2