Nevus
Symptom Information:
Symptom ID: | HPO:0003764 | |||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |