Melanocytic nevus

Symptom Information:

Symptom ID: HPO:0000995
Synonyms:
Melanocytic nevi [HPO:0000995]
Nevocellular nevi [HPO:0000995]
Pigmented naevi [HPO:0000995]
Pigmented nevus [Orphanet:23550]
Melanocytic nevus of skin (disorder) [Orphanet:23550]
Pigmented nevus, no ICD-O subtype (morphologic abnormality) [Orphanet:23550]
Melanocytic nevus (disorder) [Orphanet:23550]
Benign melanocytic nevus [Orphanet:23550]
Melanocytic nevus [Orphanet:23550]
Pigmented nevi [OMIM:Pigmented nevi]
Pigmented naevi/naevus pigmentosus/lentigo [Orphanet:23550]
Melanocytic naevus [Orphanet:23550]
Melanocytic naevus [MedDRA:10027145]
Blue naevus [MedDRA:10027145]
Halo naevus [MedDRA:10027145]
Junctional naevus [MedDRA:10027145]
Mole of skin [MedDRA:10027145]
Naevi melanocytic [MedDRA:10027145]
Naevi pigmented [MedDRA:10027145]
Naevus [MedDRA:10027145]
Nervus melanocytic [MedDRA:10027145]
Nervus pigmented [MedDRA:10027145]
Nevus [MedDRA:10027145]
Nevus melanotic [MedDRA:10027145]
Pigmented naevus [MedDRA:10027145]
Intradermal naevus [MedDRA:10027145]
Mole changes [MedDRA:10027145]
Nevus cell nevus [MedDRA:10027145]
Compound nevus [MedDRA:10027145]
Naevus cell naevus [MedDRA:10027145]
Compound naevus [MedDRA:10027145]
Intradermal nevus [MedDRA:10027145]
Blue nevus [MedDRA:10027145]
Halo nevus [MedDRA:10027145]
Junctional nevus [MedDRA:10027145]
Melanocytic nevus [MedDRA:10027145]
Pigmented nevus [MedDRA:10027145]
Mucosal pigmented naevus [MedDRA:10027145]
Mucosal pigmented nevus [MedDRA:10027145]
Naevus melanotic [MedDRA:10027145]
Blue nevi [OMIM:Blue nevi]
Halo nevi [OMIM:Halo nevi]
Pigmented nevus (rare) [OMIM:Pigmented nevus (rare)]
Lentigo [MedDRA:10024217]
Lentigo (disorder) [Orphanet:23550]
Lentiginosis (disorder) [Orphanet:23550]
Lentigo [Orphanet:23550]
Quality:
Cross references:
HPO:0007481 "Hyperpigmented nevi" [Orphanet:23550]
HPO:0003764 "Nevus" [Orphanet:23550]
Orphanet:23550 "Pigmented naevi/naevus pigmentosus/lentigo" [Orphanet:23550]
OMIM: "Pigmented nevi" [OMIM:Pigmented nevi]
OMIM: "Blue nevi" [OMIM:Blue nevi]
OMIM: "Halo nevi" [OMIM:Halo nevi]
OMIM: "Pigmented nevus (rare)" [OMIM:Pigmented nevus (rare)]
UMLS:C1456781 "Benign melanocytic nevus" [Orphanet:23550]
UMLS:C0027962 "Melanocytic nevus" [Orphanet:23550]
UMLS:C0023321 "Lentigo" [Orphanet:23550]
Is a (Direct Parents):
HPO         Abnormality of skin pigmentation
MedDRA Skin neoplasms benign
Orphanet Abnormality of skin pigmentation
HPO         Nevus
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the integument(HPO:0001574)
          Abnormality of the skin(HPO:0000951)
             Generalized abnormality of skin(HPO:0011354)
                Abnormality of skin morphology(HPO:0011121)
                   Abnormality of skin pigmentation(HPO:0001000)
                      Melanocytic nevus(HPO:0000995)
             Localized skin lesion(HPO:0011355)
                Nevus(HPO:0003764)
                   Melanocytic nevus(HPO:0000995)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Cutaneous neoplasms benign(MedDRA:10040899)
       Skin neoplasms benign(MedDRA:10040898)
          Melanocytic nevus(HPO:0000995)
Database Frequency: 63 / 7739
Resource:

All diseases associated with this symptom:

14q11.2 microdeletion syndrome (Orphanet:261120)
15q13.3 microdeletion syndrome (Orphanet:199318)
ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE (OMIM:101800)
ADULT syndrome (Orphanet:978)
ANE syndrome (Orphanet:157954)
Acro-oto-ocular syndrome (Orphanet:2980)
Acrodysostosis (Orphanet:950)
Acrodysostosis with multiple hormone resistance (Orphanet:280651)
Alexander disease (Orphanet:58)
Alopecia - epilepsy - pyorrhea - intellectual deficit (Orphanet:1008)
Angio-osteohypertrophic syndrome (Orphanet:2346)
Arterial dissection - lentiginosis (Orphanet:1682)
Arthrogryposis-like syndrome (Orphanet:1149)
Beckwith-Wiedemann syndrome (Orphanet:116)
Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11 (Orphanet:96193)
Buschke-Ollendorff syndrome (Orphanet:1306)
CARNEY COMPLEX, TYPE 1 (OMIM:160980)
Camptodactyly syndrome, Guadalajara type 1 (Orphanet:1327)
Carney complex (Orphanet:1359)
Congenital amegakaryocytic thrombocytopenia (Orphanet:3319)
Cowden syndrome (Orphanet:201)
Crouzon disease (Orphanet:207)
Crouzon syndrome - acanthosis nigricans (Orphanet:93262)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Cutis marmorata telangiectatica congenita (Orphanet:1556)
Deafness - small bowel diverticulosis - neuropathy (Orphanet:3217)
Dermo-odonto dysplasia (Orphanet:1660)
Distal monosomy 17q (Orphanet:1597)
Ectodermal dysplasia, tricho-odonto-onychial type (Orphanet:1818)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Epidermolytic ichthyosis (Orphanet:312)
FACES syndrome (Orphanet:1969)
Gastrocutaneous syndrome (Orphanet:2069)
Gorlin syndrome (Orphanet:377)
HERMANSKY-PUDLAK SYNDROME 1 (OMIM:203300)
Hermansky-Pudlak syndrome (Orphanet:79430)
Hermansky-Pudlak syndrome with pulmonary fibrosis (Orphanet:231500)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Hypo- and hypermelanotic cutaneous macules - retarded growth - intellectual deficiency (Orphanet:2435)
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia (Orphanet:1882)
Hypotrichosis with juvenile macular degeneration (Orphanet:1573)
Intellectual deficit, X-linked - cubitus valgus - dysmorphism (Orphanet:85280)
Juvenile Paget disease (Orphanet:2801)
Linear nevus sebaceus syndrome (Orphanet:2612)
NEVUS, EPIDERMAL (OMIM:162900)
Neurocutaneous melanocytosis (Orphanet:2481)
Neurofibromatosis type 1 (Orphanet:636)
Noonan syndrome (Orphanet:648)
Noonan syndrome with multiple lentigines (Orphanet:500)
Oculocutaneous albinism type 1B (Orphanet:79434)
Otodental syndrome (Orphanet:2791)
Peutz-Jeghers syndrome (Orphanet:2869)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
Progeria - short stature - pigmented nevi (Orphanet:2959)
Proteus syndrome (Orphanet:744)
Proteus-like syndrome (Orphanet:2969)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Torticollis - keloids - cryptorchidism - renal dysplasia (Orphanet:3341)
Tricho-odonto-onychial dysplasia (Orphanet:3355)
Turner syndrome (Orphanet:881)
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 (OMIM:193200)
Xeroderma pigmentosum (Orphanet:910)