Congenital localized absence of skin

Symptom Information:

Symptom ID: HPO:0007383
Synonyms:
Congenital localized skin absence [HPO:0007383]
Congenital localized absence of skin [OMIM:Congenital localized absence of skin]
Quality:
Cross references:
OMIM: "Congenital localized absence of skin" [OMIM:Congenital localized absence of skin]
Is a (Direct Parents):
HPO         Aplasia/Hypoplasia of the skin
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)
                Aplasia/Hypoplasia of the skin(HPO:0008065)
                   Congenital localized absence of skin(HPO:0007383)
MedDRA:
Database Frequency: 2 / 7739
Resource:

All diseases associated with this symptom:

EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN ANDDEFORMITY OF NAILS (OMIM:132000)
Junctional epidermolysis bullosa, Herlitz type (Orphanet:79404)