Hypermelanotic macule
Symptom Information:
Symptom ID: | HPO:0001034 | ||||||
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) Hypermelanotic macule(HPO:0001034) Generalized abnormality of skin(HPO:0011354) Abnormality of skin morphology(HPO:0011121) Abnormality of skin pigmentation(HPO:0001000) Hyperpigmentation of the skin(HPO:0000953) Irregular hyperpigmentation(HPO:0007400) Hypermelanotic macule(HPO:0001034) MedDRA: |
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Database Frequency: | 22 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
Blue rubber bleb nevus | (Orphanet:1059) |
Constitutional mismatch repair deficiency syndrome | (Orphanet:252202) |
Darier disease | (Orphanet:218) |
Dyschromatosis symmetrica hereditaria | (Orphanet:41) |
Familial progressive hyperpigmentation | (Orphanet:79146) |
HAIRY PALMS AND SOLES | (OMIM:139650) |
HYPERPIGMENTATION WITH OR WITHOUT HYPOPIGMENTATION, FAMILIAL PROGRESSIVE | (OMIM:145250) |
Hyperimmunoglobulinemia D with periodic fever | (Orphanet:343) |
Hypo- and hypermelanotic cutaneous macules - retarded growth - intellectual deficiency | (Orphanet:2435) |
Kaposi's sarcoma | (Orphanet:33276) |
LENTIGINOSIS, INHERITED PATTERNED | (OMIM:151001) |
Leigh syndrome | (Orphanet:506) |
Leprechaunism | (Orphanet:508) |
Lymphangioleiomyomatosis | (Orphanet:538) |
Maculopapular cutaneous mastocytosis | (Orphanet:79457) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
Peutz-Jeghers syndrome | (Orphanet:2869) |
SPONDYLOENCHONDRODYSPLASIA WITH IMMUNE DYSREGULATION | (OMIM:607944) |
Schimke immuno-osseous dysplasia | (Orphanet:1830) |
Torg-Winchester syndrome | (Orphanet:3460) |
[DEL] PSEUDOXANTHOMA ELASTICUM | (OMIM:264800) |