Sparse and thin eyebrow

Symptom Information:

Symptom ID: HPO:0000535
Synonyms:
Hypotrichosis of eyebrow [HPO:0000535]
SPARSE EYEBROWS [HPO:0000535]
Thin eyebrows [HPO:0000535]
Thin, sparse eyebrows [HPO:0000535]
Madarosis of eyebrow (disorder) [Orphanet:6100]
Madarosis of eyebrow [Orphanet:6100]
Sparse eyebrows [OMIM:Sparse eyebrows]
Thin eyebrows [OMIM:Thin eyebrows]
Thin, sparse eyebrows [OMIM:Thin, sparse eyebrows]
Absent/decreased/thin eyebrows [Orphanet:6100]
Eyebrows sparse [OMIM:Eyebrows sparse]
Sparse eyebrows (in some patients) [OMIM:Sparse eyebrows (in some patients)]
Sparse eyebrows (rare) [OMIM:Sparse eyebrows (rare)]
Sparse, thin eyebrows [OMIM:Sparse, thin eyebrows]
Thin eyebrows (laterally) [OMIM:Thin eyebrows (laterally)]
Quality:
Cross references:
Orphanet:6100 "Absent/decreased/thin eyebrows" [Orphanet:6100]
OMIM: "Sparse eyebrows" [OMIM:Sparse eyebrows]
OMIM: "Thin eyebrows" [OMIM:Thin eyebrows]
OMIM: "Thin, sparse eyebrows" [OMIM:Thin, sparse eyebrows]
OMIM: "Eyebrows sparse" [OMIM:Eyebrows sparse]
OMIM: "Sparse eyebrows (in some patients)" [OMIM:Sparse eyebrows (in some patients)]
OMIM: "Sparse eyebrows (rare)" [OMIM:Sparse eyebrows (rare)]
OMIM: "Sparse, thin eyebrows" [OMIM:Sparse, thin eyebrows]
OMIM: "Thin eyebrows (laterally)" [OMIM:Thin eyebrows (laterally)]
UMLS:C0578682 "Madarosis of eyebrow" [Orphanet:6100]
Is a (Direct Parents):
Orphanet Abnormality of the eyebrow
HPO         Aplasia/Hypoplasia of the eyebrow
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)
                Abnormality of the eyebrow(HPO:0000534)
                   Aplasia/Hypoplasia of the eyebrow(HPO:0100840)
                      Sparse and thin eyebrow(HPO:0000535)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the periorbital region(HPO:0000606)
                   Abnormality of the eyebrow(HPO:0000534)
                      Aplasia/Hypoplasia of the eyebrow(HPO:0100840)
                         Sparse and thin eyebrow(HPO:0000535)
                obsolete Abnormality of the ocular region(HPO:0000284)
                   Abnormality of the eyebrow(HPO:0000534)
                      Aplasia/Hypoplasia of the eyebrow(HPO:0100840)
                         Sparse and thin eyebrow(HPO:0000535)
MedDRA:
Database Frequency: 76 / 7739
Resource:

All diseases associated with this symptom:

17q12 microdeletion syndrome (Orphanet:261265)
19q13.11 microdeletion syndrome (Orphanet:217346)
8q22.1 microdeletion syndrome (Orphanet:178303)
AREDYLD syndrome (Orphanet:1133)
Autosomal dominant hypohidrotic ectodermal dysplasia (Orphanet:1810)
Autosomal recessive hypohidrotic ectodermal dysplasia (Orphanet:248)
Barber-Say syndrome (Orphanet:1231)
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency (Orphanet:329255)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
CARPENTER SYNDROME 2 (OMIM:614976)
CEREBELLOFACIODENTAL SYNDROME (OMIM:616202)
CHST3-related skeletal dysplasia (Orphanet:263463)
Cartilage-hair hypoplasia (Orphanet:175)
Cerebro-facio-thoracic dysplasia (Orphanet:1394)
Cerebro-oculo-nasal syndrome (Orphanet:66625)
Congenital nephrotic syndrome-interstitial lung disease-epidermolysis bullosa syndrome (Orphanet:306504)
Craniosynostosis - anal anomalies - porokeratosis (Orphanet:85199)
DK1-CDG (Orphanet:91131)
ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE (OMIM:614929)
ECTODERMAL DYSPLASIA SYNDROME WITH DISTINCTIVE FACIAL APPEARANCE ANDPREAXIAL POLYDACTYLY OF FEET (OMIM:129540)
ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY (OMIM:600906)
ECTODERMAL DYSPLASIA, SENSORINEURAL HEARING LOSS, AND DISTINCTIVEFACIAL FEATURES (OMIM:609944)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME1 (OMIM:129900)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
EEC syndrome (Orphanet:1896)
EEM syndrome (Orphanet:1897)
Ectodermal dysplasia - syndactyly syndrome (Orphanet:247820)
Ectodermal dysplasia with natal teeth, Turnpenny type (Orphanet:69083)
Frontonasal dysplasia with alopecia and genital anomaly (Orphanet:228390)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Glomerulonephritis - sparse hair - telangiectasis (Orphanet:2087)
HYPOTRICHOSIS 6 (OMIM:607903)
HYPOTRICHOSIS 7 (OMIM:604379)
HYPOTRICHOSIS 8 (OMIM:278150)
Hair defect - photosensitivity - intellectual deficit (Orphanet:1408)
Hallermann-Streiff syndrome (Orphanet:2108)
Hidrotic ectodermal dysplasia (Orphanet:189)
Hyperlysinemia, type I (OMIM:238700)
Hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia (Orphanet:1882)
Hypotrichosis simplex (Orphanet:55654)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11 (OMIM:602400)
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS (OMIM:602540)
Ichthyosis-hypotrichosis syndrome (Orphanet:91132)
KABUKI SYNDROME 1 (OMIM:147920)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (OMIM:612843)
KERATOSIS FOLLICULARIS SPINULOSA DECALVANS, X-LINKED (OMIM:308800)
KID syndrome (Orphanet:477)
Kabuki syndrome (Orphanet:2322)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
MACS syndrome (Orphanet:217335)
MICROCEPHALIC OSTEODYSPLASTIC PRIMORDIAL DWARFISM, TYPE I (OMIM:210710)
Marie Unna hereditary hypotrichosis (Orphanet:444)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Mucolipidosis type 2 (Orphanet:576)
NOONAN SYNDROME 4 (OMIM:610733)
Naxos disease (Orphanet:34217)
Nestor-Guillermo progeria syndrome (Orphanet:280576)
Netherton syndrome (Orphanet:634)
Oculocerebrofacial syndrome, Kaufman type (Orphanet:2707)
Odonto-onycho-dermal dysplasia (Orphanet:2721)
PACHYONYCHIA CONGENITA 2 (OMIM:167210)
PALMOPLANTAR KERATODERMA AND WOOLLY HAIR (OMIM:616099)
Premature ageing appearance-developmental delay-cardiac arrhythmia syndrome (Orphanet:276432)
Rosselli-Gulienetti syndrome (Orphanet:90339)
SHORT STATURE WITH MICROCEPHALY AND DISTINCTIVE FACIES (OMIM:615789)
SIMOSA CRANIOFACIAL SYNDROME (OMIM:182150)
STORM SYNDROME (OMIM:185069)
Skin fragility-woolly hair-palmoplantar keratoderma syndrome (Orphanet:293165)
TRICHORHINOPHALANGEAL SYNDROME, TYPE I (OMIM:190350)
Tetrasomy 12p (Orphanet:884)
Trichodysplasia - xeroderma (Orphanet:3361)
Wiedemann-Rautenstrauch syndrome (Orphanet:3455)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)
X-linked hypohidrotic ectodermal dysplasia (Orphanet:181)
Yunis-Varon syndrome (Orphanet:3472)
Zlotogora-Ogur syndrome (Orphanet:3253)