Generalized hypotrichosis
Symptom Information:
Symptom ID: | HPO:0004528 | ||||||||||||||||||||||||||||||||||||||||||
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) Generalized hypotrichosis(HPO:0004528) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin appendage conditions(MedDRA:10040798) Generalized hypotrichosis(HPO:0004528) Hypotrichosis(HPO:0001006) Generalized hypotrichosis(HPO:0004528) |
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Database Frequency: | 18 / 7739 | ||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AREDYLD syndrome | (Orphanet:1133) |
Argininosuccinic aciduria | (Orphanet:23) |
Bathing suit ichthyosis | (Orphanet:100976) |
CARASIL | (Orphanet:199354) |
Classical phenylketonuria | (Orphanet:79254) |
ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE | (OMIM:614931) |
Flynn-Aird syndrome | (Orphanet:2047) |
Hallermann-Streiff syndrome | (Orphanet:2108) |
Hawkinsinuria | (Orphanet:2118) |
Menkes disease | (Orphanet:565) |
Oculotrichodysplasia | (Orphanet:2718) |
Scalp-ear-nipple syndrome | (Orphanet:2036) |
Schöpf-Schulz-Passarge syndrome | (Orphanet:50944) |
Steinert myotonic dystrophy | (Orphanet:273) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR | (OMIM:600785) |
Werner syndrome | (Orphanet:902) |
Wilson-Turner syndrome | (Orphanet:3459) |
Woodhouse-Sakati syndrome | (Orphanet:3464) |