Hypotrichosis
Symptom Information:
Symptom ID: | HPO:0001006 | |||||||||||||||||||||||||||||||||||||||||||||
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) MedDRA: Skin and subcutaneous tissue disorders(MedDRA:10040785) Skin appendage conditions(MedDRA:10040798) Hypotrichosis(HPO:0001006) |
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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) |