Nevus

Symptom Information:

Symptom ID: HPO:0003764
Synonyms:
Naevi [HPO:0003764]
Naevus [HPO:0003764]
Nevi [HPO:0003764]
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]
Nevi [OMIM: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:0000995 "Pigmented nevi" [Orphanet:23550]
Orphanet:23550 "Pigmented naevi/naevus pigmentosus/lentigo" [Orphanet:23550]
OMIM: "Nevi" [OMIM: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):
Orphanet Abnormality of skin pigmentation
MedDRA Skin neoplasms benign
HPO         Localized skin lesion
Orphanet Melanocytic 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)
             Localized skin lesion(HPO:0011355)
                Nevus(HPO:0003764)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Cutaneous neoplasms benign(MedDRA:10040899)
       Skin neoplasms benign(MedDRA:10040898)
          Nevus(HPO:0003764)
Database Frequency: 17 / 7739
Resource:

All diseases associated with this symptom:

Bazex-Dupré-Christol syndrome (Orphanet:113)
Becker nevus syndrome (Orphanet:64755)
Buschke-Ollendorff syndrome (Orphanet:1306)
CAMPTODACTYLY SYNDROME, GUADALAJARA, TYPE III (OMIM:611929)
CARNEY COMPLEX, TYPE 1 (OMIM:160980)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carney complex (Orphanet:1359)
Costello syndrome (Orphanet:3071)
Elastosis perforans serpiginosa (Orphanet:79148)
Faciocardiorenal syndrome (Orphanet:1973)
Langer-Giedion syndrome (Orphanet:502)
Mulibrey nanism (Orphanet:2576)
NEVUS ANEMICUS (OMIM:163050)
Proteus syndrome (Orphanet:744)
SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY (OMIM:614800)
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 6 (OMIM:193200)
Vitiligo-associated autoimmune disease (Orphanet:247871)