Hypohidrotic ectodermal dysplasia
Symptom Information:
Symptom ID: | HPO:0007607 | ||
Synonyms: |
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Quality: | |||
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) Generalized abnormality of skin(HPO:0011354) Ectodermal dysplasia(HPO:0000968) Hypohidrotic ectodermal dysplasia(HPO:0007607) MedDRA: |
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Database Frequency: | 5 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal recessive hypohidrotic ectodermal dysplasia | (Orphanet:248) |
ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALDOMINANT | (OMIM:614940) |
Ectodermal dysplasia - intellectual deficit - central nervous system malformation | (Orphanet:1812) |
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia | (Orphanet:1882) |
X-linked hypohidrotic ectodermal dysplasia | (Orphanet:181) |