Alopecia

Symptom Information:

Symptom ID: HPO:0001596
Synonyms:
Hair loss [HPO:0001596]
Alopecia (disorder) [Orphanet:24160]
Loss of hair (finding) [Orphanet:24160]
Alopecia [Orphanet:24160]
Alopecia [OMIM:Alopecia]
Hair loss [OMIM:Hair loss]
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)]
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]
Quality:
Cross references:
HPO:0002289 "Alopecia universalis" [Orphanet:24160]
Orphanet:24160 "Alopecia" [Orphanet:24160]
Orphanet:24480 "Abnormal fall of hair" [Orphanet:24480]
OMIM: "Alopecia" [OMIM:Alopecia]
OMIM: "Hair loss" [OMIM:Hair loss]
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: "Thin hair (in some patients)" [OMIM:Thin hair (in some patients)]
UMLS:C0002170 "Alopecia" [HPO:0001596]
UMLS:C0002170 "Alopecia" [Orphanet:24160]
Is a (Direct Parents):
MedDRA Hypotrichosis
Orphanet Abnormality of the hair
HPO         Abnormal hair quantity
MedDRA Skin appendage conditions
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)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin appendage conditions(MedDRA:10040798)
       Hypotrichosis(HPO:0001006)
          Alopecia(HPO:0001596)
       Alopecia(HPO:0001596)
Database Frequency: 162 / 7739
Resource:

All diseases associated with this symptom:

17q11.2 microduplication syndrome (Orphanet:139474)
3-@METHYLCROTONYL-CoA CARBOXYLASE 2 DEFICIENCY (OMIM:210210)
ADULT syndrome (Orphanet:978)
ALOPECIA, ANDROGENETIC, 1 (OMIM:109200)
ALOPECIA, CONGENITAL (OMIM:300042)
ANE syndrome (Orphanet:157954)
Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
Adams-Oliver syndrome (Orphanet:974)
Albright hereditary osteodystrophy (Orphanet:665)
Alopecia (Orphanet:79364)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Alopecia - epilepsy - pyorrhea - intellectual deficit (Orphanet:1008)
Alopecia - intellectual deficit - hypergonadotropic hypogonadism (Orphanet:1014)
Alopecia totalis (Orphanet:700)
Alopecia universalis (Orphanet:701)
Alopecia-intellectual deficit syndrome (Orphanet:2850)
Alpha heavy-chain disease (Orphanet:100025)
Alström syndrome (Orphanet:64)
Argininosuccinic aciduria (Orphanet:23)
Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant hypocalcemia (Orphanet:428)
Autosomal dominant palmoplantar keratoderma and congenital alopecia (Orphanet:1010)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive hypohidrotic ectodermal dysplasia (Orphanet:248)
BRESEK syndrome (Orphanet:85284)
Bathing suit ichthyosis (Orphanet:100976)
Biotinidase deficiency (Orphanet:79241)
Björnstad syndrome (Orphanet:123)
CANDIDIASIS, FAMILIAL, 1 (OMIM:114580)
CARASIL (Orphanet:199354)
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 (OMIM:212750)
CHILD syndrome (Orphanet:139)
Cerebellar ataxia - ectodermal dysplasia (Orphanet:1174)
Chronic mucocutaneous candidiasis (Orphanet:1334)
Classical mycosis fungoides (Orphanet:2584)
Congenital erythropoietic porphyria (Orphanet:79277)
Congenital non-bullous ichthyosiform erythroderma (Orphanet:79394)
Cortisone reductase deficiency 1 (OMIM:604931)
Crandall syndrome (Orphanet:202)
Cronkhite-Canada syndrome (Orphanet:2930)
DK1-CDG (Orphanet:91131)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 1 (OMIM:127550)
DYSKERATOSIS CONGENITA, AUTOSOMAL DOMINANT, 3 (OMIM:613990)
Deafness - genital anomalies - metacarpal and metatarsal synostosis (Orphanet:3224)
Deafness-craniofacial syndrome (Orphanet:3241)
Distal monosomy 19p13.3 (Orphanet:96129)
Dorfman-Chanarin disease (Orphanet:98907)
Dyskeratosis congenita (Orphanet:1775)
ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE (OMIM:602032)
ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE (OMIM:614931)
ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET (OMIM:129540)
Ehlers-Danlos syndrome, progeroid type (Orphanet:75496)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Epidermolysis bullosa simplex due to plakophilin deficiency (Orphanet:158668)
Epidermolysis bullosa simplex with anodontia/hypodontia (Orphanet:2325)
Epidermolysis bullosa simplex with muscular dystrophy (Orphanet:257)
Erosive pustular dermatosis of the scalp (Orphanet:222)
Erythrokeratodermia variabilis (Orphanet:317)
Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome (Orphanet:313846)
Fibrodysplasia ossificans progressiva (Orphanet:337)
Flynn-Aird syndrome (Orphanet:2047)
Focal dermal hypoplasia (Orphanet:2092)
Frontonasal dysplasia with alopecia and genital anomaly (Orphanet:228390)
GAPO syndrome (Orphanet:2067)
Giant cell arteritis (Orphanet:397)
Glomerulonephritis - sparse hair - telangiectasis (Orphanet:2087)
Graham Little-Piccardi-Lassueur syndrome (Orphanet:505)
Gómez-López-Hernández syndrome (Orphanet:1532)
HYPOTRICHOSIS 4 (OMIM:146550)
Hallermann-Streiff syndrome (Orphanet:2108)
Hemochromatosis, type 1 (OMIM:235200)
Hepatoerythropoietic porphyria (Orphanet:95159)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hidrotic ectodermal dysplasia (Orphanet:189)
Holocarboxylase synthetase deficiency (Orphanet:79242)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Hyperandrogenism due to cortisone reductase deficiency (Orphanet:168588)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Hypotrichosis - lymphedema - telangiectasia (Orphanet:69735)
Hypotrichosis simplex (Orphanet:55654)
ICHTHYOSIFORM ERYTHRODERMA, CORNEAL INVOLVEMENT, AND DEAFNESS (OMIM:242150)
IMMUNODEFICIENCY, COMMON VARIABLE, 10 (OMIM:615577)
Ichthyosis - alopecia - eclabion - ectropion - intellectual deficit (Orphanet:2269)
Ichthyosis - hypotrichosis - sclerosing cholangitis (Orphanet:59303)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Immunodeficiency due to CD25 deficiency (Orphanet:169100)
Incontinentia pigmenti (Orphanet:464)
Ito hypomelanosis (Orphanet:435)
Johanson-Blizzard syndrome (Orphanet:2315)
Junctional epidermolysis bullosa (Orphanet:305)
Junctional epidermolysis bullosa, Herlitz type (Orphanet:79404)
Juvenile dermatomyositis (Orphanet:93672)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (OMIM:612843)
Keratoderma hereditarium mutilans (Orphanet:494)
Keratosis follicularis - dwarfism - cerebral atrophy (Orphanet:2339)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
Kerion celsi (Orphanet:499)
Keutel syndrome (Orphanet:85202)
Lethal acantholytic epidermolysis bullosa (Orphanet:158687)
Lichen planopilaris (Orphanet:525)
Linear nevus sebaceus syndrome (Orphanet:2612)
Loose anagen syndrome (Orphanet:168)
MACS syndrome (Orphanet:217335)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibuloacral dysplasia with type A lipodystrophy (Orphanet:90153)
Marie Unna hereditary hypotrichosis (Orphanet:444)
Mixed connective tissue disease (Orphanet:809)
Monilethrix (Orphanet:573)
Moynahan syndrome (Orphanet:2574)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Neuroectodermal-endocrine syndrome (Orphanet:2676)
Oculocerebrocutaneous syndrome (Orphanet:1647)
Odonto-onycho dysplasia - alopecia (Orphanet:2722)
Omenn syndrome (Orphanet:39041)
Orofaciodigital syndrome type 1 (Orphanet:2750)
PARC syndrome (Orphanet:2825)
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 4 (OMIM:615830)
POIKILODERMA, HEREDITARY FIBROSING, WITH TENDON CONTRACTURES, MYOPATHY,AND PULMONARY FIBROSIS (OMIM:615704)
Pachyonychia congenita (Orphanet:2309)
Pearson syndrome (Orphanet:699)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Pili torti (Orphanet:2889)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Primary cutaneous lymphoma (Orphanet:542)
Primary hypergonadotropic hypogonadism - partial alopecia (Orphanet:2232)
Pseudo-pelade of Brocq (Orphanet:129)
Pure hair and nail ectodermal dysplasia (Orphanet:69084)
Quinquaud's folliculitis decalvans (Orphanet:346)
Recessive dystrophic epidermolysis bullosa inversa (Orphanet:79409)
Recessive dystrophic epidermolysis bullosa-generalized other (Orphanet:89842)
Rhizomelic chondrodysplasia punctata (Orphanet:177)
Rhizomelic chondrodysplasia punctata type 1 (Orphanet:309789)
Rothmund-Thomson syndrome (Orphanet:2909)
Scalp-ear-nipple syndrome (Orphanet:2036)
Schöpf-Schulz-Passarge syndrome (Orphanet:50944)
Severe T-cell immunodeficiency - congenital alopecia - nail dystrophy (Orphanet:169095)
Severe combined immunodeficiency (Orphanet:183660)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Sinus node disease and myopia (OMIM:182190)
Skin fragility-woolly hair-palmoplantar keratoderma syndrome (Orphanet:293165)
Sézary syndrome (Orphanet:3162)
TRAPS syndrome (Orphanet:32960)
TRICHOTILLOMANIA (OMIM:613229)
Thumb deformity - alopecia - pigmentation anomaly (Orphanet:2251)
Thymoma (Orphanet:99867)
Transgrediens et progrediens palmoplantar keratoderma (Orphanet:495)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Trichodysplasia - xeroderma (Orphanet:3361)
Ulerythema ophryogenesis (Orphanet:3406)
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR (OMIM:600785)
Werner syndrome (Orphanet:902)
Woodhouse-Sakati syndrome (Orphanet:3464)
Wrinkly skin syndrome (Orphanet:2834)
X-linked agammaglobulinemia (Orphanet:47)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)
Xeroderma pigmentosum (Orphanet:910)
Zlotogora-Ogur syndrome (Orphanet:3253)