DISEASES Neoplasms [C04] Neoplasms Neoplasms by Histologic Type [C04.557] Neoplasms by Histologic Type Nevi and Melanomas [C04.557.665] Nevi and Melanomas Nevus [C04.557.665.560] Nevus Dysplastic Nevus Syndrome [C04.557.665.560.260] Dysplastic Nevus Syndrome Nevus, Halo [C04.557.665.560.580] Nevus, Halo Nevus, Intradermal [C04.557.665.560.590] Nevus, Intradermal Nevus, Pigmented [C04.557.665.560.615] Nevus, Pigmented Nevus, Sebaceous of Jadassohn [C04.557.665.560.700] Nevus, Sebaceous of Jadassohn DISEASES Nervous System Diseases [C10] Nervous System Diseases Neurocutaneous Syndromes [C10.562] Neurocutaneous Syndromes Ataxia Telangiectasia [C10.562.100] Ataxia Telangiectasia Neurofibromatoses [C10.562.600] Neurofibromatoses Nevus, Sebaceous of Jadassohn [C10.562.700] Nevus, Sebaceous of Jadassohn Sturge-Weber Syndrome [C10.562.800] Sturge-Weber Syndrome Tuberous Sclerosis [C10.562.850] Tuberous Sclerosis von Hippel-Lindau Disease [C10.562.925] von Hippel-Lindau Disease DISEASES Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Congenital, Hereditary, and Neonatal Diseases and Abnormalities Congenital Abnormalities [C16.131] Congenital Abnormalities Abnormalities, Multiple [C16.131.077] Abnormalities, Multiple 22q11 Deletion Syndrome [C16.131.077.019] 22q11 Deletion Syndrome Alagille Syndrome [C16.131.077.065] Alagille Syndrome Angelman Syndrome [C16.131.077.095] Angelman Syndrome Barth Syndrome [C16.131.077.121] Barth Syndrome Basal Cell Nevus Syndrome [C16.131.077.130] Basal Cell Nevus Syndrome Beckwith-Wiedemann Syndrome [C16.131.077.133] Beckwith-Wiedemann Syndrome Bloom Syndrome [C16.131.077.137] Bloom Syndrome Branchio-Oto-Renal Syndrome [C16.131.077.208] Branchio-Oto-Renal Syndrome Carney Complex [C16.131.077.229] Carney Complex Ciliopathies [C16.131.077.245] Ciliopathies Cockayne Syndrome [C16.131.077.250] Cockayne Syndrome Costello Syndrome [C16.131.077.256] Costello Syndrome Cri-du-Chat Syndrome [C16.131.077.262] Cri-du-Chat Syndrome De Lange Syndrome [C16.131.077.272] De Lange Syndrome Deaf-Blind Disorders [C16.131.077.299] Deaf-Blind Disorders Donohue Syndrome [C16.131.077.313] Donohue Syndrome Down Syndrome [C16.131.077.327] Down Syndrome Ectodermal Dysplasia [C16.131.077.350] Ectodermal Dysplasia Fraser Syndrome [C16.131.077.371] Fraser Syndrome Gardner Syndrome [C16.131.077.393] Gardner Syndrome Heterotaxy Syndrome [C16.131.077.401] Heterotaxy Syndrome Holoprosencephaly [C16.131.077.410] Holoprosencephaly Incontinentia Pigmenti [C16.131.077.445] Incontinentia Pigmenti Isolated Noncompaction of the Ventricular Myocardium [C16.131.077.477] Isolated Noncompaction of the Ventricular Myocardium Laurence-Moon Syndrome [C16.131.077.509] Laurence-Moon Syndrome LEOPARD Syndrome [C16.131.077.525] LEOPARD Syndrome Loeys-Dietz Syndrome [C16.131.077.537] Loeys-Dietz Syndrome Marfan Syndrome [C16.131.077.550] Marfan Syndrome Mobius Syndrome [C16.131.077.578] Mobius Syndrome Monilethrix [C16.131.077.592] Monilethrix Nail-Patella Syndrome [C16.131.077.606] Nail-Patella Syndrome Netherton Syndrome [C16.131.077.619] Netherton Syndrome Nevus, Sebaceous of Jadassohn [C16.131.077.633] Nevus, Sebaceous of Jadassohn Oculocerebrorenal Syndrome [C16.131.077.662] Oculocerebrorenal Syndrome Orofaciodigital Syndromes [C16.131.077.676] Orofaciodigital Syndromes Pallister-Hall Syndrome [C16.131.077.690] Pallister-Hall Syndrome Pentalogy of Cantrell [C16.131.077.696] Pentalogy of Cantrell POEMS Syndrome [C16.131.077.703] POEMS Syndrome Polycystic Kidney Diseases [C16.131.077.717] Polycystic Kidney Diseases Prader-Willi Syndrome [C16.131.077.730] Prader-Willi Syndrome Prolidase Deficiency [C16.131.077.735] Prolidase Deficiency Proteus Syndrome [C16.131.077.740] Proteus Syndrome Prune Belly Syndrome [C16.131.077.745] Prune Belly Syndrome Rubella Syndrome, Congenital [C16.131.077.790] Rubella Syndrome, Congenital Rubinstein-Taybi Syndrome [C16.131.077.804] Rubinstein-Taybi Syndrome Short Rib-Polydactyly Syndrome [C16.131.077.850] Short Rib-Polydactyly Syndrome Silver-Russell Syndrome [C16.131.077.855] Silver-Russell Syndrome Smith-Lemli-Opitz Syndrome [C16.131.077.860] Smith-Lemli-Opitz Syndrome Smith-Magenis Syndrome [C16.131.077.879] Smith-Magenis Syndrome Sotos Syndrome [C16.131.077.889] Sotos Syndrome Trichothiodystrophy Syndromes [C16.131.077.899] Trichothiodystrophy Syndromes Trisomy 13 Syndrome [C16.131.077.919] Trisomy 13 Syndrome Trisomy 18 Syndrome [C16.131.077.929] Trisomy 18 Syndrome Waardenburg Syndrome [C16.131.077.938] Waardenburg Syndrome Weill-Marchesani Syndrome [C16.131.077.941] Weill-Marchesani Syndrome Wolf-Hirschhorn Syndrome [C16.131.077.944] Wolf-Hirschhorn Syndrome Zellweger Syndrome [C16.131.077.970] Zellweger Syndrome

Nevus, Sebaceous of Jadassohn - Preferred

Concept UI	M0499750
Scope note	A syndrome characterized by lesions occurring on the face, scalp, or neck which consist of congenital hypoplastic malformations of cutaneous structures and which over time undergo verrucous hyperplasia. Additionally it is associated with neurological symptoms and skeletal, ophthalmological, urogenital, and cardiovascular abnormalities.
Preferred term	Nevus, Sebaceous of Jadassohn
Entry term(s)	Jadassohn Nevus Phakomatosis Jadassohn Nevus Sebaceus Jadassohn Sebaceous Nevus Linear Sebaceous Nevus Linear Sebaceous Nevus Syndrome Nevus Phakomatosis, Jadassohn Nevus Sebaceus of Jadassohn Nevus, Linear Sebaceous Phakomatosis, Jadassohn Nevus Sebaceous Nevus Syndrome, Linear Sebaceous Nevus of Jadassohn Sebaceous Nevus, Linear

Linear Verrucous Epidermal Nevus - Related but not broader or narrower

Concept UI	M0552398
Preferred term	Linear Verrucous Epidermal Nevus
Entry term(s)	Epidermal Nevus, Verrucous Nevus, Verrucous Epidermal Verrucous Epidermal Nevus

Verrucous Nevus - Related but not broader or narrower

Concept UI	M0531003
Preferred term	Verrucous Nevus
Entry term(s)	Nevus, Verrucous

Inflammatory Linear Verrucose Epidermal Nevus - Related but not broader or narrower

Concept UI	M0552397
Preferred term	Inflammatory Linear Verrucose Epidermal Nevus
Entry term(s)	Inflammatory Linear Verrucous Epidermal Naevus

Organoid Nevus Phakomatosis - Related but not broader or narrower

Concept UI	M0499754
Preferred term	Organoid Nevus Phakomatosis
Entry term(s)	Feuerstein Mims Syndrome Feuerstein-Mims Syndrome Nevus Phakomatoses, Organoid Nevus Phakomatosis, Organoid Organoid Nevus Phakomatoses Phakomatoses, Organoid Nevus Phakomatosis, Organoid Nevus Schimmelpenning Feuerstein Mims Syndrome Schimmelpenning Syndrome Schimmelpenning-Feuerstein-Mims Syndrome Syndrome, Feuerstein-Mims Syndrome, Schimmelpenning Syndrome, Schimmelpenning-Feuerstein-Mims