Hypotrichosis of the scalp
Symptom Information:
Symptom ID: | HPO:0004782 | |||||
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 skin adnexa(HPO:0011138) Abnormality of the hair(HPO:0001595) Abnormal hair quantity(HPO:0011362) Hypotrichosis(HPO:0001006) Hypotrichosis of the scalp(HPO:0004782) MedDRA: |
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Database Frequency: | 7 / 7739 | |||||
Resource: |
All diseases associated with this symptom:
AREDYLD syndrome | (Orphanet:1133) |
Generalized basaloid follicular hamartoma syndrome | (Orphanet:168632) |
HYPOTRICHOSIS 2 | (OMIM:146520) |
HYPOTRICHOSIS 3 | (OMIM:613981) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hereditary sensory and autonomic neuropathy type 4 | (Orphanet:642) |
Hypotrichosis simplex of the scalp | (Orphanet:90368) |