Alopecia universalis
Symptom Information:
Symptom ID: | HPO:0002289 | |||||||||||||||||||||||||||||||||
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 skin adnexa(HPO:0011138) Abnormality of the hair(HPO:0001595) Abnormal hair quantity(HPO:0011362) Alopecia(HPO:0001596) Alopecia universalis(HPO:0002289) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin appendage conditions(MedDRA:10040798) Hypotrichosis(HPO:0001006) Alopecia universalis(HPO:0002289) Alopecia universalis(HPO:0002289) |
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Database Frequency: | 20 / 7739 | |||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
ALOPECIA AREATA 1 | (OMIM:104000) |
ALOPECIA UNIVERSALIS CONGENITA | (OMIM:203655) |
ALOPECIA-MENTAL RETARDATION SYNDROME 1 | (OMIM:203650) |
ALOPECIA-MENTAL RETARDATION SYNDROME 2 | (OMIM:610422) |
ALOPECIA-MENTAL RETARDATION SYNDROME 3 | (OMIM:613930) |
Alopecia - epilepsy - pyorrhea - intellectual deficit | (Orphanet:1008) |
Alopecia-intellectual deficit syndrome | (Orphanet:2850) |
Alström syndrome | (Orphanet:64) |
Bathing suit ichthyosis | (Orphanet:100976) |
CARASIL | (Orphanet:199354) |
ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE | (OMIM:614931) |
Flynn-Aird syndrome | (Orphanet:2047) |
Hemochromatosis, type 1 | (OMIM:235200) |
Hypocalcemic vitamin D-resistant rickets | (Orphanet:93160) |
Mutilating palmoplantar keratoderma with periorificial keratotic plaques | (Orphanet:659) |
SATOYOSHI SYNDROME | (OMIM:600705) |
Scalp-ear-nipple syndrome | (Orphanet:2036) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR | (OMIM:600785) |
Werner syndrome | (Orphanet:902) |
Woodhouse-Sakati syndrome | (Orphanet:3464) |