Alopecia universalis

Symptom Information:

Symptom ID: HPO:0002289
Synonyms:
Alopecia, complete [HPO:0002289]
Alopecia [Orphanet:24160]
Alopecia (disorder) [Orphanet:24160]
Loss of hair (finding) [Orphanet:24160]
Alopecia universalis [OMIM:Alopecia universalis]
Alopecia, complete [OMIM:Alopecia, complete]
Alopecia [MedDRA:10001760]
Accelerated hair loss [MedDRA:10001760]
Alopecia reversible [MedDRA:10001760]
Alopecia, unspecified [MedDRA:10001760]
Atrichia [MedDRA:10001760]
Atrichosis [MedDRA:10001760]
Baldness [MedDRA:10001760]
Frontal-parietal thinning [MedDRA:10001760]
Hair loss [MedDRA:10001760]
Hair thinning [MedDRA:10001760]
Other alopecia [MedDRA:10001760]
Body hair loss [MedDRA:10001760]
Traction alopecia [MedDRA:10001760]
Alopecia post chemotherapy [MedDRA:10001760]
Alopecia (in 1 patient) [OMIM:Alopecia (in 1 patient)]
Alopecia (in some patients) [OMIM:Alopecia (in some patients)]
Alopecia (occurs before neurologic signs) [OMIM:Alopecia (occurs before neurologic signs)]
Alopecia universalis (entire loss of all hair on body) [OMIM:Alopecia universalis (entire loss of all hair on body)]
Alopecia universalis (in some patients) [OMIM:Alopecia universalis (in some patients)]
Atrichia [OMIM:Atrichia]
Baldness [OMIM:Baldness]
Thin hair (in some patients) [OMIM:Thin hair (in some patients)]
Abnormal fall of hair [Orphanet:24480]
Abnormal hair loss [Orphanet:24480]
Alopecia (disorder) [Orphanet:24480]
Alopecias [MedDRA:10001769]
Alopecia universalis [MedDRA:10001767]
Quality:
Cross references:
HPO:0001596 "Alopecia" [Orphanet:24160]
Orphanet:24160 "Alopecia" [Orphanet:24160]
Orphanet:24480 "Abnormal fall of hair" [Orphanet:24480]
OMIM: "Alopecia universalis" [OMIM:Alopecia universalis]
OMIM: "Alopecia, complete" [OMIM:Alopecia, complete]
OMIM: "Alopecia (in 1 patient)" [OMIM:Alopecia (in 1 patient)]
OMIM: "Alopecia (in some patients)" [OMIM:Alopecia (in some patients)]
OMIM: "Alopecia (occurs before neurologic signs)" [OMIM:Alopecia (occurs before neurologic signs)]
OMIM: "Alopecia universalis (entire loss of all hair on body)" [OMIM:Alopecia universalis (entire loss of all hair on body)]
OMIM: "Alopecia universalis (in some patients)" [OMIM:Alopecia universalis (in some patients)]
OMIM: "Atrichia" [OMIM:Atrichia]
OMIM: "Baldness" [OMIM:Baldness]
OMIM: "Thin hair (in some patients)" [OMIM:Thin hair (in some patients)]
UMLS:C0002170 "Alopecia" [Orphanet:24160]
Is a (Direct Parents):
MedDRA Skin appendage conditions
MedDRA Hypotrichosis
Orphanet Abnormality of the hair
HPO         Alopecia
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)
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)