Melanocytic nevus
Symptom Information:
Symptom ID: | HPO:0000995 | |||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
|
|||||||||||||||||||||||||||||||||||||||||||||||
Quality: | ||||||||||||||||||||||||||||||||||||||||||||||||
Cross references: |
|
|||||||||||||||||||||||||||||||||||||||||||||||
Is a (Direct Parents): |
|
|||||||||||||||||||||||||||||||||||||||||||||||
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) Melanocytic nevus(HPO:0000995) Generalized abnormality of skin(HPO:0011354) Abnormality of skin morphology(HPO:0011121) Abnormality of skin pigmentation(HPO:0001000) 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) |