Aplasia cutis congenita
Symptom Information:
Symptom ID: | HPO:0001057 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
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) |