Hypotrichosis

Symptom Information:

Symptom ID: HPO:0001006
Synonyms:
Congenital hypotrichosis [HPO:0001006]
Hypotrichosis, infantile [HPO:0001006]
Marked hypotrichosis [HPO:0001006]
Atrichia (disorder) [Orphanet:24080]
Hypotrichosis (disorder) [Orphanet:24080]
Alopecia (disorder) [Orphanet:24080]
Loss of hair (finding) [Orphanet:24080]
Alopecia [Orphanet:24080]
Atrichia [Orphanet:24080]
Hypotrichosis [Orphanet:24080]
Congenital hypotrichosis [OMIM:Congenital hypotrichosis]
Hypotrichosis [OMIM:Hypotrichosis]
Marked hypotrichosis [OMIM:Marked hypotrichosis]
Hypotrichosis/atrichia/atrichiasis/scalp hairlessness [Orphanet:24080]
Atrichosis [Orphanet:24080]
Hypotrichosis [MedDRA:10021126]
Hypotrichosis of eyelid [MedDRA:10021126]
Facial hair decreased [MedDRA:10021126]
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]
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:0004528 "Generalized hypotrichosis" [Orphanet:24080]
Orphanet:24080 "Hypotrichosis/atrichia/atrichiasis/scalp hairlessness" [Orphanet:24080]
Orphanet:24480 "Abnormal fall of hair" [Orphanet:24480]
OMIM: "Congenital hypotrichosis" [OMIM:Congenital hypotrichosis]
OMIM: "Hypotrichosis" [OMIM:Hypotrichosis]
OMIM: "Marked hypotrichosis" [OMIM:Marked hypotrichosis]
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:C0020678 "Hypotrichosis" [HPO:0001006]
UMLS:C0002170 "Alopecia" [Orphanet:24080]
UMLS:C0702167 "Atrichia" [Orphanet:24080]
UMLS:C0020678 "Hypotrichosis" [Orphanet:24080]
Is a (Direct Parents):
HPO         Abnormal hair quantity
MedDRA Skin appendage conditions
Orphanet Abnormality of the hair
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)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin appendage conditions(MedDRA:10040798)
       Hypotrichosis(HPO:0001006)
Database Frequency: 219 / 7739
Resource:

All diseases associated with this symptom:

19q13.11 microdeletion syndrome (Orphanet:217346)
2q32q33 microdeletion syndrome (Orphanet:251019)
2q37 microdeletion syndrome (Orphanet:1001)
8q22.1 microdeletion syndrome (Orphanet:178303)
ADULT syndrome (Orphanet:978)
ALOPECIA, CONGENITAL (OMIM:300042)
AREDYLD syndrome (Orphanet:1133)
Ablepharon macrostomia syndrome (Orphanet:920)
Absent thumb - short stature - immunodeficiency (Orphanet:2951)
Ackerman syndrome (Orphanet:2561)
Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
Acrofacial dysostosis, Palagonia type (Orphanet:1787)
Adams-Oliver syndrome (Orphanet:974)
Alopecia (Orphanet:79364)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Alopecia - epilepsy - pyorrhea - intellectual deficit (Orphanet:1008)
Alopecia antibody deficiency (Orphanet:1006)
Alopecia totalis (Orphanet:700)
Alopecia universalis (Orphanet:701)
Alopecia-intellectual deficit syndrome (Orphanet:2850)
Aniridia - ptosis - intellectual deficit - familial obesity (Orphanet:1067)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Aplasia cutis congenita - intestinal lymphangiectasia (Orphanet:1116)
Argininosuccinic aciduria (Orphanet:23)
Atrichia with papular lesions (Orphanet:86819)
Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Autoimmune polyendocrinopathy type 2 (Orphanet:3143)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal dominant palmoplantar keratoderma and congenital alopecia (Orphanet:1010)
Autosomal recessive hypohidrotic ectodermal dysplasia (Orphanet:248)
Bamforth syndrome (Orphanet:1226)
Bartsocas-Papas syndrome (Orphanet:1234)
Bathing suit ichthyosis (Orphanet:100976)
Bazex-Dupré-Christol syndrome (Orphanet:113)
Biotinidase deficiency (Orphanet:79241)
Bird headed-dwarfism, Montreal type (Orphanet:2617)
Blepharo-cheilo-odontic syndrome (Orphanet:1997)
Bullous dystrophy, macular type (Orphanet:1867)
CARASIL (Orphanet:199354)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carney complex (Orphanet:1359)
Cartilage-hair hypoplasia (Orphanet:175)
Cerebellar ataxia - ectodermal dysplasia (Orphanet:1174)
Choroidal atrophy - alopecia (Orphanet:1433)
Classical homocystinuria (Orphanet:394)
Classical phenylketonuria (Orphanet:79254)
Cleft lip/palate - deafness - sacral lipoma (Orphanet:2003)
Cockayne syndrome (Orphanet:191)
Congenital short bowel syndrome (Orphanet:2301)
Crandall syndrome (Orphanet:202)
Cranioectodermal dysplasia (Orphanet:1515)
Craniolenticulosutural dysplasia (Orphanet:50814)
Cronkhite-Canada syndrome (Orphanet:2930)
Deafness - enamel hypoplasia - nail defects (Orphanet:3220)
Deafness-craniofacial syndrome (Orphanet:3241)
Dermatomyositis (Orphanet:221)
Dermo-odonto dysplasia (Orphanet:1660)
Desbuquois syndrome (Orphanet:1425)
Distal trisomy 6p (Orphanet:1745)
Down syndrome (Orphanet:870)
Dubowitz syndrome (Orphanet:235)
Dyskeratosis congenita (Orphanet:1775)
ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT (OMIM:129490)
ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMALRECESSIVE (OMIM:224900)
ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE (OMIM:614929)
ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE (OMIM:614931)
ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE (OMIM:129810)
EEM syndrome (Orphanet:1897)
Ectodermal dysplasia - blindness (Orphanet:1806)
Ectodermal dysplasia - cutaneous syndactyly syndrome (Orphanet:247827)
Ectodermal dysplasia - sensorineural deafness (Orphanet:1883)
Ectodermal dysplasia syndrome (Orphanet:79373)
Ectodermal dysplasia, Berlin type (Orphanet:1816)
Ectodermal dysplasia, tricho-odonto-onychial type (Orphanet:1818)
Ehlers-Danlos syndrome, vascular type (Orphanet:286)
Ellis Van Creveld syndrome (Orphanet:289)
Epidermolysis bullosa simplex due to plakophilin deficiency (Orphanet:158668)
Epidermolysis bullosa simplex with anodontia/hypodontia (Orphanet:2325)
Facial ectodermal dysplasia (Orphanet:1807)
Familial benign copper deficiency (Orphanet:1551)
Fibrodysplasia ossificans progressiva (Orphanet:337)
Flynn-Aird syndrome (Orphanet:2047)
GAPO syndrome (Orphanet:2067)
Genitopatellar syndrome (Orphanet:85201)
Glomerulonephritis - sparse hair - telangiectasis (Orphanet:2087)
Goldberg-Shprintzen megacolon syndrome (Orphanet:66629)
Graham Little-Piccardi-Lassueur syndrome (Orphanet:505)
Gómez-López-Hernández syndrome (Orphanet:1532)
HYPOTRICHOSIS 1 (OMIM:605389)
HYPOTRICHOSIS 11 (OMIM:615059)
HYPOTRICHOSIS 12 (OMIM:615885)
HYPOTRICHOSIS 13 (OMIM:615896)
HYPOTRICHOSIS 4 (OMIM:146550)
HYPOTRICHOSIS 6 (OMIM:607903)
HYPOTRICHOSIS 7 (OMIM:604379)
Hair defect - photosensitivity - intellectual deficit (Orphanet:1408)
Hallermann-Streiff syndrome (Orphanet:2108)
Hawkinsinuria (Orphanet:2118)
Hereditary hypotrichosis with recurrent skin vesicles (Orphanet:217407)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hidrotic ectodermal dysplasia, Christianson-Fourie type (Orphanet:1808)
Hidrotic ectodermal dysplasia, Halal type (Orphanet:1809)
Hoyeraal-Hreidarsson syndrome (Orphanet:3322)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Hypogonadotropic hypogonadism - frontoparietal alopecia (Orphanet:2230)
Hypohidrotic ectodermal dysplasia (Orphanet:238468)
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia (Orphanet:1882)
Hypotrichosis - lymphedema - telangiectasia (Orphanet:69735)
Hypotrichosis simplex (Orphanet:55654)
Hypotrichosis with juvenile macular degeneration (Orphanet:1573)
Ichthyosis - alopecia - eclabion - ectropion - intellectual deficit (Orphanet:2269)
Ichthyosis - hypotrichosis - sclerosing cholangitis (Orphanet:59303)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Ichthyosis-hypotrichosis syndrome (Orphanet:91132)
Intellectual deficit - balding - patella luxation - acromicria (Orphanet:3041)
Intellectual deficit - sparse hair - brachydactyly (Orphanet:3051)
KID syndrome (Orphanet:477)
Kaler-Garrity-Stern syndrome (Orphanet:2324)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
Lamellar ichthyosis (Orphanet:313)
Langer-Giedion syndrome (Orphanet:502)
Linear nevus sebaceus syndrome (Orphanet:2612)
Linear verrucous nevus syndrome (Orphanet:2611)
Lipodystrophy due to peptidic growth factors deficiency (Orphanet:1979)
Lipoid proteinosis (Orphanet:530)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibuloacral dysplasia with type B lipodystrophy (Orphanet:90154)
Marie Unna hereditary hypotrichosis (Orphanet:444)
Marshall syndrome (Orphanet:560)
Menkes disease (Orphanet:565)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Monilethrix (Orphanet:573)
Moynahan syndrome (Orphanet:2574)
Multiple non-ossifying fibromatosis (Orphanet:2029)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
Naxos disease (Orphanet:34217)
Netherton syndrome (Orphanet:634)
Neuroectodermal syndrome, Johnson type (Orphanet:2316)
Neuroectodermal-endocrine syndrome (Orphanet:2676)
Nijmegen breakage syndrome (Orphanet:647)
Non-rhizomelic chondrodysplasia punctata (Orphanet:176)
Noonan syndrome (Orphanet:648)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
Oculocerebrorenal syndrome (Orphanet:534)
Oculodentodigital dysplasia (Orphanet:2710)
Oculoosteocutaneous syndrome (Orphanet:2713)
Oculotrichodysplasia (Orphanet:2718)
Odonto-onycho dysplasia - alopecia (Orphanet:2722)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
Odontotrichomelic syndrome (Orphanet:2723)
Oley syndrome (Orphanet:79458)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Osteoporosis - pseudoglioma (Orphanet:2788)
PARC syndrome (Orphanet:2825)
POEMS syndrome (Orphanet:2905)
Pachyonychia congenita (Orphanet:2309)
Papillon-Lefèvre syndrome (Orphanet:678)
Paraplegia - intellectual deficit - hyperkeratosis (Orphanet:2824)
Paternal 20q13.2q13.3 microdeletion syndrome (Orphanet:261304)
Pierre Robin syndrome - faciodigital anomaly (Orphanet:2888)
Pili torti - onychodysplasia (Orphanet:2890)
Pilodental dysplasia - refractive errors (Orphanet:2892)
Primary hypergonadotropic hypogonadism - partial alopecia (Orphanet:2232)
Progeroid syndrome, Petty type (Orphanet:2963)
Prolidase deficiency (Orphanet:742)
Proliferating trichilemmal cyst (Orphanet:492)
Pseudo-pelade of Brocq (Orphanet:129)
Renpenning syndrome (Orphanet:3242)
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications (Orphanet:3018)
Retinopathy - anemia- central nervous system anomalies (Orphanet:3088)
Rhizomelic chondrodysplasia punctata (Orphanet:177)
Rhizomelic syndrome, Urbach type (Orphanet:3098)
Roberts syndrome (Orphanet:3103)
Rothmund-Thomson syndrome (Orphanet:2909)
Rothmund-Thomson syndrome type 1 (Orphanet:221008)
Rothmund-Thomson syndrome type 2 (Orphanet:221016)
SABINAS BRITTLE HAIR SYNDROME (OMIM:211390)
SCARF syndrome (Orphanet:3134)
SHORT syndrome (Orphanet:3163)
Scalp defects - postaxial polydactyly (Orphanet:1003)
Scalp-ear-nipple syndrome (Orphanet:2036)
Schöpf-Schulz-Passarge syndrome (Orphanet:50944)
Seckel syndrome (Orphanet:808)
Severe dermatitis-multiple allergies-metabolic wasting syndrome (Orphanet:369992)
Sparse hair - short stature - skin anomalies (Orphanet:79132)
Spondyloepimetaphyseal dysplasia - hypotrichosis (Orphanet:168443)
Steinert myotonic dystrophy (Orphanet:273)
Syringocystadenoma papilliferum (Orphanet:840)
TETRAAMELIA WITH ECTODERMAL DYSPLASIA AND LACRIMAL DUCT ABNORMALITIES (OMIM:273390)
Taurodontia - absent teeth - sparse hair (Orphanet:2731)
Teebi-Shaltout syndrome (Orphanet:3291)
Tetrasomy 12p (Orphanet:884)
Thrombocytopenia - Robin sequence (Orphanet:3323)
Thumb deformity - alopecia - pigmentation anomaly (Orphanet:2251)
Tricho-oculo-dermo-vertebral syndrome (Orphanet:3354)
Tricho-odonto-onychial dysplasia (Orphanet:3355)
Tricho-odonto-onychodysplasia - dominant syndactyly (Orphanet:3357)
Tricho-retino-dento-digital syndrome (Orphanet:1264)
Trichodermal syndrome - intellectual deficit (Orphanet:3360)
Trichodermodysplasia - dental alterations (Orphanet:3353)
Trichodysplasia - amelogenesis imperfecta (Orphanet:79129)
Trichodysplasia - xeroderma (Orphanet:3361)
Trichomegaly - retina pigmentary degeneration - dwarfism (Orphanet:3363)
Trichorhinophalangeal syndrome type 1 and 3 (Orphanet:77258)
Uncombable hair syndrome (Orphanet:1410)
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR (OMIM:600785)
Vogt-Koyanagi-Harada disease (Orphanet:3437)
Weaver-Williams syndrome (Orphanet:3448)
Werner syndrome (Orphanet:902)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
Wilson-Turner syndrome (Orphanet:3459)
Woodhouse-Sakati syndrome (Orphanet:3464)
Woolly hair - hypotrichosis - everted lower lip - outstanding ears (Orphanet:1409)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
Yunis-Varon syndrome (Orphanet:3472)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)
Zlotogora-Ogur syndrome (Orphanet:3253)
Zunich-Kaye syndrome (Orphanet:3474)