Adermatoglyphia
Symptom Information:
Symptom ID: | HPO:0007455 | ||
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) Regional abnormality of skin(HPO:0011356) Abnormal dermatoglyphics(HPO:0007477) Adermatoglyphia(HPO:0007455) MedDRA: |
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Database Frequency: | 4 / 7739 | ||
Resource: |
All diseases associated with this symptom:
ADULT syndrome | (Orphanet:978) |
Absence of fingerprints - congenital milia | (Orphanet:1658) |
Dermatopathia pigmentosa reticularis | (Orphanet:86920) |
Isolated adermatoglyphia | (Orphanet:289465) |