Aplasia cutis congenita

Symptom Information:

Symptom ID: HPO:0001057
Synonyms:
Aplasia cutis congenita [OMIM:Aplasia cutis congenita]
Aplasia cutis congenita [MedDRA:10002963]
Quality:
Cross references:
OMIM: "Aplasia cutis congenita" [OMIM:Aplasia cutis congenita]
Is a (Direct Parents):
MedDRA Skin hyperplasias and hypertrophies
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)
                   Aplasia cutis congenita(HPO:0001057)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Cornification and dystrophic skin disorders(MedDRA:10011063)
       Skin hyperplasias and hypertrophies(MedDRA:10040866)
          Aplasia cutis congenita(HPO:0001057)
Database Frequency: 7 / 7739
Resource:

All diseases associated with this symptom:

ADAMS-OLIVER SYNDROME 5 (OMIM:616028)
Acrofacial dysostosis, Palagonia type (Orphanet:1787)
Branchio-oculo-facial syndrome (Orphanet:1297)
Junctional epidermolysis bullosa - pyloric atresia (Orphanet:79403)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Recessive aplasia cutis congenita of limbs (Orphanet:1115)
Toriello-Lacassie-Droste syndrome (Orphanet:3339)