Generalized hypotrichosis

Symptom Information:

Symptom ID: HPO:0004528
Synonyms:
Hypotrichosis, generalized [HPO:0004528]
Hypotrichosis [Orphanet:24080]
Atrichia (disorder) [Orphanet:24080]
Hypotrichosis (disorder) [Orphanet:24080]
Alopecia (disorder) [Orphanet:24080]
Loss of hair (finding) [Orphanet:24080]
Alopecia [Orphanet:24080]
Atrichia [Orphanet:24080]
Generalized hypotrichosis [OMIM:Generalized hypotrichosis]
Hypotrichosis, generalized [OMIM:Hypotrichosis, generalized]
Hypotrichosis/atrichia/atrichiasis/scalp hairlessness [Orphanet:24080]
Atrichosis [Orphanet:24080]
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]
Hypotrichosis [MedDRA:10021126]
Hypotrichosis of eyelid [MedDRA:10021126]
Facial hair decreased [MedDRA:10021126]
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)]
Atrichia [OMIM:Atrichia]
Baldness [OMIM:Baldness]
Hypotrichosis (especially scalp, eyebrows, and eyelashes) [OMIM:Hypotrichosis (especially scalp, eyebrows, and eyelashes)]
Hypotrichosis (in some patients) [OMIM:Hypotrichosis (in some patients)]
Hypotrichosis (scalp) [OMIM:Hypotrichosis (scalp)]
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]
Quality:
Cross references:
HPO:0001006 "Hypotrichosis" [Orphanet:24080]
Orphanet:24080 "Hypotrichosis/atrichia/atrichiasis/scalp hairlessness" [Orphanet:24080]
Orphanet:24480 "Abnormal fall of hair" [Orphanet:24480]
OMIM: "Generalized hypotrichosis" [OMIM:Generalized hypotrichosis]
OMIM: "Hypotrichosis, generalized" [OMIM:Hypotrichosis, generalized]
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: "Atrichia" [OMIM:Atrichia]
OMIM: "Baldness" [OMIM:Baldness]
OMIM: "Hypotrichosis (especially scalp, eyebrows, and eyelashes)" [OMIM:Hypotrichosis (especially scalp, eyebrows, and eyelashes)]
OMIM: "Hypotrichosis (in some patients)" [OMIM:Hypotrichosis (in some patients)]
OMIM: "Hypotrichosis (scalp)" [OMIM:Hypotrichosis (scalp)]
OMIM: "Thin hair (in some patients)" [OMIM:Thin hair (in some patients)]
UMLS:C0002170 "Alopecia" [Orphanet:24080]
UMLS:C0702167 "Atrichia" [Orphanet:24080]
UMLS:C0020678 "Hypotrichosis" [Orphanet:24080]
Is a (Direct Parents):
MedDRA Hypotrichosis
Orphanet Hypotrichosis
Orphanet Abnormality of the hair
MedDRA Skin appendage conditions
HPO         Hypotrichosis
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)
       Hypotrichosis(HPO:0001006)
          Generalized hypotrichosis(HPO:0004528)
       Generalized hypotrichosis(HPO:0004528)
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)