Aplasia cutis congenita of scalp
Symptom Information:
Symptom ID: | HPO:0007385 | ||||||||
Synonyms: |
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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) 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: |
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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) |