Axillary freckling

Symptom Information:

Symptom ID: HPO:0000997
Synonyms:
Axillary freckling [OMIM:Axillary freckling]
Quality:
Cross references:
OMIM: "Axillary freckling" [OMIM:Axillary freckling]
Is a (Direct Parents):
HPO         Freckling
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:
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)