Aplasia cutis congenita of scalp

Symptom Information:

Symptom ID: HPO:0007385
Synonyms:
Defect of scalp [HPO:0007385]
Scalp aplasia cutis congenita [HPO:0007385]
Scalp defect [HPO:0007385]
Aplasia cutis congenita of scalp [OMIM:Aplasia cutis congenita of scalp]
Scalp aplasia cutis congenita [OMIM:Scalp aplasia cutis congenita]
Scalp defect [OMIM:Scalp defect]
Scalp defect. [OMIM:Scalp defect.]
Scalp defects [OMIM:Scalp defects]
Quality:
Cross references:
OMIM: "Aplasia cutis congenita of scalp" [OMIM:Aplasia cutis congenita of scalp]
OMIM: "Scalp aplasia cutis congenita" [OMIM:Scalp aplasia cutis congenita]
OMIM: "Scalp defect" [OMIM:Scalp defect]
OMIM: "Scalp defect." [OMIM:Scalp defect.]
OMIM: "Scalp defects" [OMIM:Scalp defects]
Is a (Direct Parents):
HPO         Aplasia cutis congenita
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)
                      Aplasia cutis congenita of scalp(HPO:0007385)
MedDRA:
Database Frequency: 10 / 7739
Resource:

All diseases associated with this symptom:

BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED, WITH APLASIACUTIS CONGENITA (OMIM:302803)
ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY (OMIM:600906)
Johanson-Blizzard syndrome (Orphanet:2315)
PARIETAL FORAMINA (OMIM:168500)
PARIETAL FORAMINA 2 (OMIM:609597)
PARIETAL FORAMINA 3 (OMIM:609566)
Parietal foramina (Orphanet:60015)
Scalp defects - postaxial polydactyly (Orphanet:1003)
Wolf-Hirschhorn syndrome (Orphanet:280)