Numerous pigmented freckles
Symptom Information:
| Symptom ID: | HPO:0007587 | ||||
| Synonyms: |
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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) Generalized abnormality of skin(HPO:0011354) Abnormality of skin morphology(HPO:0011121) Abnormality of skin pigmentation(HPO:0001000) Numerous pigmented freckles(HPO:0007587) MedDRA: |
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| Database Frequency: | 22 / 7739 | ||||
| Resource: |
All diseases associated with this symptom:
| ADULT syndrome | (Orphanet:978) |
| Cryptomicrotia - brachydactyly - excess fingertip arch | (Orphanet:1547) |
| Deaf blind hypopigmentation syndrome, Yemenite type | (Orphanet:3214) |
| Dwarfism - intellectual deficit - eye abnormality | (Orphanet:2650) |
| Dyschromatosis symmetrica hereditaria | (Orphanet:41) |
| Dyschromatosis universalis | (Orphanet:241) |
| Familial melanoma | (Orphanet:618) |
| Hypotrichosis with juvenile macular degeneration | (Orphanet:1573) |
| Neurofibromatosis type 1 | (Orphanet:636) |
| Neurofibromatosis type 6 | (Orphanet:2678) |
| Nijmegen breakage syndrome | (Orphanet:647) |
| Noonan syndrome with multiple lentigines | (Orphanet:500) |
| Oculocutaneous albinism type 1A | (Orphanet:79431) |
| Oculocutaneous albinism type 1B | (Orphanet:79434) |
| Oculocutaneous albinism type 2 | (Orphanet:79432) |
| Oculocutaneous albinism type 3 | (Orphanet:79433) |
| Progeria - short stature - pigmented nevi | (Orphanet:2959) |
| Pseudoprogeria syndrome | (Orphanet:2985) |
| X-linked recessive ocular albinism | (Orphanet:54) |
| Xeroderma pigmentosum | (Orphanet:910) |
| Xeroderma pigmentosum complementation group F | (Orphanet:276264) |
| Xeroderma pigmentosum variant | (Orphanet:90342) |