Axillary freckling
Symptom Information:
Symptom ID: | HPO:0000997 | ||
Synonyms: |
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Quality: | |||
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) Freckling(HPO:0001480) Axillary freckling(HPO:0000997) MedDRA: |
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Database Frequency: | 9 / 7739 | ||
Resource: |
All diseases associated with this symptom:
17q11 microdeletion syndrome | (Orphanet:97685) |
17q11.2 microduplication syndrome | (Orphanet:139474) |
Constitutional mismatch repair deficiency syndrome | (Orphanet:252202) |
Legius syndrome | (Orphanet:137605) |
Neurofibromatosis type 1 due to NF1mutation or intragenic deletion | (Orphanet:363700) |
Non-polyposis Turcot syndrome | (Orphanet:99817) |
PHEOCHROMOCYTOMA--ISLET CELL TUMOR SYNDROME | (OMIM:171420) |
Watson syndrome | (Orphanet:3444) |
[DEL] NEUROFIBROMATOSIS-NOONAN SYNDROME | (OMIM:601321) |