Multiple cafe-au-lait spots
Symptom Information:
Symptom ID: | HPO:0007565 | |||||||||
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) 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) Cafe-au-lait spot(HPO:0000957) Multiple cafe-au-lait spots(HPO:0007565) Localized skin lesion(HPO:0011355) Hypermelanotic macule(HPO:0001034) Cafe-au-lait spot(HPO:0000957) Multiple cafe-au-lait spots(HPO:0007565) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Pigmentation disorders(MedDRA:10035023) Hyperpigmentation disorders(MedDRA:10020713) Multiple cafe-au-lait spots(HPO:0007565) |
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Database Frequency: | 11 / 7739 | |||||||||
Resource: |
All diseases associated with this symptom:
17q11 microdeletion syndrome | (Orphanet:97685) |
17q11.2 microduplication syndrome | (Orphanet:139474) |
Bloom syndrome | (Orphanet:125) |
FANCONI ANEMIA, COMPLEMENTATION GROUP G | (OMIM:614082) |
FANCONI ANEMIA, COMPLEMENTATION GROUP J | (OMIM:609054) |
LEOPARD SYNDROME 3 | (OMIM:613707) |
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 | (OMIM:614114) |
Neuroectodermal syndrome, Johnson type | (Orphanet:2316) |
Neurofibromatosis type 6 | (Orphanet:2678) |
Severe congenital hypochromic anemia with ringed sideroblasts | (Orphanet:300298) |
Watson syndrome | (Orphanet:3444) |