Input | HPO ID | HPO term | Distance | Gene | Gene id entrez | HGNC ID | DiseaseId | DiseaseName | Frequency | Onset | HGMD variants | ClinVar variants |
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HPO disease - gene - phenotype typical associations: |
HPO disease - gene - phenotype less frequent non-typical associations: |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | AARS1 CL E G H | 16 | 20 | OMIM:619691 | TRICHOTHIODYSTROPHY 8, NONPHOTOSENSITIVE; TTD8 | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | ALX1 CL E G H | 8092 | 1494 | ORPHA:306542 | Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome | HP:0040282 - Frequent | | | 5 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | ALX4 CL E G H | 60529 | 450 | OMIM:613451 | Frontonasal dysplasia 2 | | | | 132 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | ANTXR1 CL E G H | 84168 | 21014 | ORPHA:2067 | GAPO syndrome | | | | 8 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | ANTXR1 CL E G H | 84168 | 21014 | OMIM:230740 | Gapo syndrome | . | | | 8 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | APCDD1 CL E G H | 147495 | 15718 | OMIM:605389 | Hypotrichosis 1 | HP:0040284 - Very rare | | | 1 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | APCDD1 CL E G H | 147495 | 15718 | ORPHA:55654 | Hypotrichosis simplex | | | | 1 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | ATAD3A CL E G H | 55210 | 25567 | OMIM:618810 | PONTOCEREBELLAR HYPOPLASIA, HYPOTONIA, AND RESPIRATORY INSUFFICIENCY SYNDROME, NEONATAL LETHAL; PHRINL | | | | 5 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | ATR CL E G H | 545 | 882 | OMIM:614564 | Cutaneous telangiectasia and cancer syndrome, familial | | | | 168 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | B4GALT7 CL E G H | 11285 | 930 | ORPHA:75496 | B4GALT7-related spondylodysplastic Ehlers-Danlos syndrome | | | | 29 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | BANF1 CL E G H | 8815 | 17397 | OMIM:614008 | Nestor-Guillermo progeria syndrome | | | | 22 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | BRF1 CL E G H | 2972 | 11551 | ORPHA:444072 | Cerebellar-facial-dental syndrome | HP:0040281 - Very frequent | | | 7 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | BRF1 CL E G H | 2972 | 11551 | OMIM:616202 | Cerebellofaciodental syndrome | | | | 7 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | CDC42 CL E G H | 998 | 1736 | ORPHA:487796 | Macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome | HP:0040283 - Occasional | | | 6 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | CDC42 CL E G H | 998 | 1736 | OMIM:616737 | Takenouchi-Kosaki syndrome | . | | | 6 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | CDC42BPB CL E G H | 9578 | 1738 | OMIM:619841 | | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | CDH3 CL E G H | 1001 | 1762 | OMIM:225280 | Ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome | | | | 87 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | CHST3 CL E G H | 9469 | 1971 | ORPHA:263463 | CHST3-related skeletal dysplasia | HP:0040281 - Very frequent | | | 165 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | CHST3 CL E G H | 9469 | 1971 | OMIM:143095 | Spondyloepiphyseal dysplasia with congenital joint dislocations | | | | 165 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | CLDN1 CL E G H | 9076 | 2032 | ORPHA:59303 | Neonatal ichthyosis-sclerosing cholangitis syndrome | | | | 11 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | COG6 CL E G H | 57511 | 18621 | ORPHA:363523 | Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome | | | | 71 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | COL11A1 CL E G H | 1301 | 2186 | ORPHA:560 | Marshall syndrome | | | | 215 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | CRIPT CL E G H | 9419 | 14312 | OMIM:615789 | Short stature with microcephaly and distinctive facies | | | | 4 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | CWC27 CL E G H | 10283 | 10664 | OMIM:250410 | Retinitis pigmentosa with or without skeletal anomalies | | | | 4 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | DLX4 CL E G H | 1748 | 2917 | OMIM:616788 | Orofacial cleft 15 | | | | 1 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | DOLK CL E G H | 22845 | 23406 | OMIM:610768 | Congenital disorder of glycosylation, type Im | | | | 55 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | DPH1 CL E G H | 1801 | 3003 | ORPHA:459061 | Craniofacial dysplasia-short stature-ectodermal anomalies-intellectual disability syndrome | HP:0040281 - Very frequent | | | 3 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | DPH1 CL E G H | 1801 | 3003 | OMIM:616901 | Developmental delay with short stature, dysmorphic features, and sparse hair | . | | | 3 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | DPH5 CL E G H | 51611 | 24270 | OMIM:620070 | | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | DSC3 CL E G H | 1825 | 3037 | OMIM:613102 | HYPOTRICHOSIS AND RECURRENT SKIN VESICLES | | | | 2 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | DSG4 CL E G H | 147409 | 21307 | OMIM:607903 | Hypotrichosis 6 | | | | 63 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | DSG4 CL E G H | 147409 | 21307 | ORPHA:55654 | Hypotrichosis simplex | | | | 63 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | DSP CL E G H | 1832 | 3052 | OMIM:607655 | Skin fragility-woolly hair syndrome | | | | 747 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | EBP CL E G H | 10682 | 3133 | OMIM:302960 | Chondrodysplasia punctata 2, X-linked dominant | | | | 51 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | EBP CL E G H | 10682 | 3133 | ORPHA:35173 | X-linked dominant chondrodysplasia punctata | | | | 51 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | EDA CL E G H | 1896 | 3157 | OMIM:305100 | Ectodermal dysplasia 1, hypohidrotic, X-linked | | | | 115 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | EDAR CL E G H | 10913 | 2895 | OMIM:129490 | Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant | | | | 86 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | EDAR CL E G H | 10913 | 2895 | OMIM:224900 | Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive | | | | 86 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | EDARADD CL E G H | 128178 | 14341 | OMIM:129490 | Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant | | | | 56 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | EDARADD CL E G H | 128178 | 14341 | OMIM:224900 | Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive | | | | 56 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | EDARADD CL E G H | 128178 | 14341 | OMIM:614941 | Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive | | | | 56 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | FIG4 CL E G H | 9896 | 16873 | OMIM:216340 | Yunis-Varon syndrome | | | | 111 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | FIG4 CL E G H | 9896 | 16873 | ORPHA:3472 | Yunis-Varon syndrome | HP:0040282 - Frequent | | | 111 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | GAD1 CL E G H | 2571 | 4092 | OMIM:619124 | DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 89; DEE89 | | | | 44 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | GJA1 CL E G H | 2697 | 4274 | ORPHA:1010 | Autosomal dominant palmoplantar keratoderma and congenital alopecia | | | | 68 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | GJA1 CL E G H | 2697 | 4274 | OMIM:104100 | Palmoplantar keratoderma with congenital alopecia | | | | 68 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | GJB2 CL E G H | 2706 | 4284 | OMIM:602540 | Ichthyosis, hystrix-like, with deafness | | | | 199 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | GJB2 CL E G H | 2706 | 4284 | OMIM:148210 | Keratitis-Ichthyosis-Deafness syndrome, autosomal dominant | | | | 199 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | GJB2 CL E G H | 2706 | 4284 | ORPHA:477 | KID syndrome | | | | 199 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | GJB6 CL E G H | 10804 | 4288 | OMIM:129500 | Clouston syndrome | | | | 56 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | GJB6 CL E G H | 10804 | 4288 | ORPHA:189 | Hidrotic ectodermal dysplasia | | | | 56 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | GJB6 CL E G H | 10804 | 4288 | ORPHA:477 | KID syndrome | | | | 56 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | GNPTAB CL E G H | 79158 | 29670 | OMIM:252500 | Mucolipidosis II alpha/beta | | | | 240 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | GTPBP2 CL E G H | 54676 | 4670 | OMIM:617988 | Jaberi-Elahi syndrome | . | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | H3-3A CL E G H | 3020 | 4764 | OMIM:619720 | BRYANT-LI-BHOJ NEURODEVELOPMENTAL SYNDROME 1; BRYLIB1 | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | H4C5 CL E G H | 8367 | 4790 | OMIM:619950 | | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | HDAC4 CL E G H | 9759 | 14063 | ORPHA:1001 | 2q37 microdeletion syndrome | | | | 33 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | HECW2 CL E G H | 57520 | 29853 | OMIM:617268 | Neurodevelopmental disorder with hypotonia, seizures, and absent language | . | | | 11 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | HEPHL1 CL E G H | 341208 | 30477 | OMIM:261990 | PILI TORTI AND DEVELOPMENTAL DELAY | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | HERC1 CL E G H | 8925 | 4867 | OMIM:617011 | Macrocephaly, dysmorphic facies, and psychomotor retardation | . | | | 16 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | HERC1 CL E G H | 8925 | 4867 | ORPHA:457359 | Megalencephaly-severe kyphoscoliosis-overgrowth syndrome | HP:0040281 - Very frequent | | | 16 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | HNRNPK CL E G H | 3190 | 5044 | OMIM:616580 | Au-Kline syndrome | | | | 8 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | HRURF CL E G H | 120766137 | 55085 | OMIM:146550 | Marie unna hereditary hypotrichosis 1 | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | IRX5 CL E G H | 10265 | 14361 | OMIM:611174 | Hamamy syndrome | | | | 4 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | ITGA3 CL E G H | 3675 | 6139 | OMIM:614748 | Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital | | | | 6 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | JUP CL E G H | 3728 | 6207 | OMIM:601214 | Naxos disease | | | | 222 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KANK2 CL E G H | 25959 | 29300 | OMIM:616099 | Palmoplantar keratoderma and woolly hair | | | | 1 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KAT5 CL E G H | 10524 | 5275 | OMIM:619103 | NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES; NEDFASB | | | | 1 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KAT6A CL E G H | 7994 | 13013 | OMIM:616268 | Arboleda-Tham syndrome | | | | 34 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KDM1A CL E G H | 23028 | 29079 | ORPHA:477993 | Palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome | HP:0040283 - Occasional | | | 3 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KDM6A CL E G H | 7403 | 12637 | ORPHA:2322 | Kabuki syndrome | | | | 53 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KDM6A CL E G H | 7403 | 12637 | OMIM:147920 | Kabuki syndrome 1 | | | | 53 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KDM6A CL E G H | 7403 | 12637 | OMIM:300867 | Kabuki syndrome 2 | | | | 53 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KIFBP CL E G H | 26128 | 23419 | ORPHA:66629 | Goldberg-Shprintzen megacolon syndrome | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KMT2D CL E G H | 8085 | 7133 | ORPHA:2322 | Kabuki syndrome | | | | 660 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KMT2D CL E G H | 8085 | 7133 | OMIM:147920 | Kabuki syndrome 1 | | | | 660 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KMT5B CL E G H | 51111 | 24283 | OMIM:617788 | Mental retardation, autosomal dominant 51 | | | | 2 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KRT17 CL E G H | 3872 | 6427 | OMIM:167210 | Pachyonychia congenita 2 | | | | 23 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KRT25 CL E G H | 147183 | 30839 | ORPHA:170 | Woolly hair | | | | 2 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KRT71 CL E G H | 112802 | 28927 | ORPHA:170 | Woolly hair | | | | 1 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KRT74 CL E G H | 121391 | 28929 | OMIM:614929 | Ectodermal dysplasia 7, Hair/nail type | | | | 5 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | KRT74 CL E G H | 121391 | 28929 | ORPHA:170 | Woolly hair | | | | 5 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | LARP7 CL E G H | 51574 | 24912 | ORPHA:319671 | Alazami syndrome | HP:0040282 - Frequent | | | 16 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | LIG4 CL E G H | 3981 | 6601 | ORPHA:235 | Dubowitz syndrome | | | | 88 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | LIPH CL E G H | 200879 | 18483 | OMIM:604379 | Hypotrichosis 7 | | | | 12 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | LIPH CL E G H | 200879 | 18483 | ORPHA:55654 | Hypotrichosis simplex | | | | 12 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | LIPH CL E G H | 200879 | 18483 | ORPHA:170 | Woolly hair | | | | 12 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | LMBRD2 CL E G H | 92255 | 25287 | OMIM:619694 | DEVELOPMENTAL DELAY WITH VARIABLE NEUROLOGIC AND BRAIN ABNORMALITIES; DENBA | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | LMNA CL E G H | 4000 | 6636 | ORPHA:1662 | Restrictive dermopathy | HP:0040281 - Very frequent | | | 645 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | LPAR6 CL E G H | 10161 | 15520 | OMIM:278150 | Hypotrichosis 8 | | | | 8 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | LPAR6 CL E G H | 10161 | 15520 | ORPHA:55654 | Hypotrichosis simplex | | | | 8 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | LPAR6 CL E G H | 10161 | 15520 | ORPHA:170 | Woolly hair | | | | 8 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | LRP1 CL E G H | 4035 | 6692 | OMIM:604093 | Keratosis pilaris atrophicans | | | | 4 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | LSS CL E G H | 4047 | 6708 | ORPHA:55654 | Hypotrichosis simplex | | | | 2 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | LZTR1 CL E G H | 8216 | 6742 | OMIM:616564 | Noonan syndrome 10 | | | | 43 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | LZTR1 CL E G H | 8216 | 6742 | OMIM:605275 | Noonan syndrome 2 | | | | 43 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | MAN1B1 CL E G H | 11253 | 6823 | ORPHA:397941 | MAN1B1-CDG | HP:0040283 - Occasional | | | 93 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | MAN1B1 CL E G H | 11253 | 6823 | OMIM:614202 | Rafiq syndrome | | | | 93 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | MAPKAPK5 CL E G H | 8550 | 6889 | OMIM:619869 | | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | MARS1 CL E G H | 4141 | 6898 | OMIM:619692 | TRICHOTHIODYSTROPHY 9, NONPHOTOSENSITIVE; TTD9 | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | MBTPS2 CL E G H | 51360 | 15455 | OMIM:308800 | Keratosis follicularis spinulosa decalvans, X-linked | | | | 22 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | MED12 CL E G H | 9968 | 11957 | OMIM:300895 | Ohdo syndrome, X-linked | | | | 228 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | MED12L CL E G H | 116931 | 16050 | OMIM:618872 | NIZON-ISIDOR SYNDROME; NIZIDS | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | MED25 CL E G H | 81857 | 28845 | ORPHA:464738 | Basel-Vanagaite-Smirin-Yosef syndrome | HP:0040282 - Frequent | | | 43 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | MEGF8 CL E G H | 1954 | 3233 | OMIM:614976 | Carpenter syndrome 2 | | | | 13 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | MEIS2 CL E G H | 4212 | 7001 | OMIM:600987 | Cleft palate, cardiac defects, and mental retardation | . | | | 7 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | MESD CL E G H | 23184 | 13520 | OMIM:618644 | OSTEOGENESIS IMPERFECTA, TYPE XX; OI20 | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | MTX2 CL E G H | 10651 | 7506 | OMIM:619127 | MANDIBULOACRAL DYSPLASIA PROGEROID SYNDROME; MDPS | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | NAA10 CL E G H | 8260 | 18704 | OMIM:300855 | Ogden syndrome | | | | 23 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | NECTIN1 CL E G H | 5818 | 9706 | OMIM:225060 | Cleft lip/palate-ectodermal dysplasia syndrome | | | | 4 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | NECTIN1 CL E G H | 5818 | 9706 | ORPHA:3253 | Cleft lip/palate-ectodermal dysplasia syndrome | | | | 4 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | NF1 CL E G H | 4763 | 7765 | ORPHA:139474 | 17q11.2 microduplication syndrome | | | | 1952 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | NFIB CL E G H | 4781 | 7785 | OMIM:618286 | Macrocephaly, acquired, with impaired intellectual development | . | | | 1 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | NSD1 CL E G H | 64324 | 14234 | OMIM:117550 | Sotos syndrome 1 | | | | 544 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | NSUN2 CL E G H | 54888 | 25994 | ORPHA:235 | Dubowitz syndrome | | | | 84 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | NUP188 CL E G H | 23511 | 17859 | OMIM:618804 | SANDESTIG-STEFANOVA SYNDROME; SANDSTEF | | | | 4 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | ODC1 CL E G H | 4953 | 8109 | ORPHA:544488 | Global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome | HP:0040283 - Occasional | | | 1 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | PIGK CL E G H | 10026 | 8965 | OMIM:618879 | NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CEREBELLAR ATROPHY, WITH OR WITHOUT SEIZURES; NEDHCAS | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | PLXNA1 CL E G H | 5361 | 9099 | OMIM:619955 | | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | POLR3A CL E G H | 11128 | 30074 | OMIM:264090 | Wiedemann-Rautenstrauch syndrome | | | | 138 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | PPP1CB CL E G H | 5500 | 9282 | OMIM:617506 | Noonan syndrome-like disorder with loose anagen hair 2 | | | | 9 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | PPP2R3C CL E G H | 55012 | 17485 | OMIM:618419 | Gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy | . | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | PQBP1 CL E G H | 10084 | 9330 | OMIM:309500 | Renpenning syndrome | | | | 28 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | PURA CL E G H | 5813 | 9701 | ORPHA:314655 | Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion | | | | 53 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | RAF1 CL E G H | 5894 | 9829 | OMIM:611553 | Noonan syndrome 5 | | | | 212 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | RECQL4 CL E G H | 9401 | 9949 | OMIM:268400 | ROTHMUND-THOMSON SYNDROME; RTS | | | | 445 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | RIN2 CL E G H | 54453 | 18750 | OMIM:613075 | Macs syndrome | | | | 43 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | RMRP CL E G H | 6023 | 10031 | ORPHA:175 | Cartilage-hair hypoplasia | | | | 37 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | RMRP CL E G H | 6023 | 10031 | OMIM:250250 | Cartilage-Hair hypoplasia | | | | 37 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | RNU4ATAC CL E G H | 100151683 | 34016 | OMIM:210710 | Microcephalic osteodysplastic primordial dwarfism, type I | | | | 15 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | RPL21 CL E G H | 6144 | 10313 | ORPHA:55654 | Hypotrichosis simplex | | | | 1 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | RPS28 CL E G H | 6234 | 10418 | OMIM:606164 | Diamond-Blackfan anemia 15 with mandibulofacial dysostosis | | | | 1 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | SIAH1 CL E G H | 6477 | 10857 | OMIM:619314 | BURATTI-HAREL SYNDROME; BURHAS | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | SMARCA2 CL E G H | 6595 | 11098 | OMIM:619293 | BLEPHAROPHIMOSIS-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME; BIS | | | | 146 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | SMARCA2 CL E G H | 6595 | 11098 | OMIM:601358 | Nicolaides-Baraitser syndrome | | | | 146 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | SMS CL E G H | 6611 | 11123 | OMIM:309583 | Mental retardation, X-linked, syndromic, Snyder-Robinson type | | | | 19 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | SMS CL E G H | 6611 | 11123 | ORPHA:3063 | X-linked intellectual disability, Snyder type | HP:0040283 - Occasional | | | 19 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | SNRPE CL E G H | 6635 | 11161 | ORPHA:55654 | Hypotrichosis simplex | | | | 2 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | SON CL E G H | 6651 | 11183 | ORPHA:500150 | Brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome | HP:0040283 - Occasional | | | 12 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | SON CL E G H | 6651 | 11183 | OMIM:617140 | Zttk syndrome | | | | 12 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | SOS1 CL E G H | 6654 | 11187 | OMIM:610733 | Noonan syndrome 4 | | | | 315 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | SOS2 CL E G H | 6655 | 11188 | OMIM:616559 | NOONAN SYNDROME 9; NS9 | | | | 30 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | SPINK5 CL E G H | 11005 | 15464 | OMIM:256500 | Netherton syndrome | | | | 100 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | SPINK5 CL E G H | 11005 | 15464 | ORPHA:634 | Netherton syndrome | | | | 100 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | SPOP CL E G H | 8405 | 11254 | OMIM:618829 | NABAIS SA-DE VRIES SYNDROME, TYPE 2; NSDVS2 | | | | 16 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | SPRED2 CL E G H | 200734 | 17722 | OMIM:619745 | NOONAN SYNDROME 14; NS14 | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | ST14 CL E G H | 6768 | 11344 | OMIM:602400 | Ichthyosis, congenital, autosomal recessive 11 | | | | 4 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | STAG2 CL E G H | 10735 | 11355 | ORPHA:521258 | Xq25 microduplication syndrome | HP:0040282 - Frequent | | | 1 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | TBCD CL E G H | 6904 | 11581 | ORPHA:496641 | Early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome | HP:0040283 - Occasional | | | 16 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | TBCD CL E G H | 6904 | 11581 | OMIM:617193 | ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN ATROPHY AND THIN CORPUS CALLOSUM; PEBAT | | | | 16 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | TBX3 CL E G H | 6926 | 11602 | OMIM:181450 | Ulnar-Mammary syndrome | | | | 100 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | TCF4 CL E G H | 6925 | 11634 | OMIM:610954 | Pitt-Hopkins syndrome | | | | 241 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | THUMPD1 CL E G H | 55623 | 23807 | OMIM:619989 | | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | TMEM147 CL E G H | 10430 | 30414 | OMIM:620075 | | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | TP63 CL E G H | 8626 | 15979 | OMIM:604292 | Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 | | | | 140 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | TP63 CL E G H | 8626 | 15979 | ORPHA:1896 | EEC syndrome | | | | 140 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | TP63 CL E G H | 8626 | 15979 | ORPHA:69085 | Limb-mammary syndrome | HP:0040284 - Very rare | | | 140 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | TP63 CL E G H | 8626 | 15979 | OMIM:129400 | Rapp-Hodgkin syndrome | | | | 140 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | TRPS1 CL E G H | 7227 | 12340 | ORPHA:77258 | Trichorhinophalangeal syndrome type 1 and 3 | | | | 171 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | TRPS1 CL E G H | 7227 | 12340 | OMIM:190350 | Trichorhinophalangeal syndrome, type I | | | | 171 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | TRPS1 CL E G H | 7227 | 12340 | OMIM:190351 | Trichorhinophalangeal syndrome, type III | | | | 171 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | TWIST2 CL E G H | 117581 | 20670 | OMIM:209885 | Barber-Say syndrome | | | | 7 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | TWIST2 CL E G H | 117581 | 20670 | ORPHA:1807 | Focal facial dermal dysplasia type III | | | | 7 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | UBE3B CL E G H | 89910 | 13478 | OMIM:244450 | Kaufman oculocerebrofacial syndrome | | | | 13 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | USB1 CL E G H | 79650 | 25792 | OMIM:604173 | Poikiloderma with neutropenia | | | | 8 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | VAC14 CL E G H | 55697 | 25507 | ORPHA:3472 | Yunis-Varon syndrome | HP:0040282 - Frequent | | | 6 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | WDR26 CL E G H | 80232 | 21208 | ORPHA:513456 | Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome | | | | 8 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | WDR26 CL E G H | 80232 | 21208 | OMIM:617616 | Skraban-Deardorff syndrome | | | | 8 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | WDR35 CL E G H | 57539 | 29250 | OMIM:613610 | Cranioectodermal dysplasia 2 | . | | | 136 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | WLS CL E G H | 79971 | 30238 | OMIM:619648 | ZAKI SYNDROME; ZKS | | | | | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | WNT10A CL E G H | 80326 | 13829 | OMIM:257980 | Odontoonychodermal dysplasia | | | | 71 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | WNT10A CL E G H | 80326 | 13829 | OMIM:150400 | Tooth agenesis, selective, 4 | HP:0040283 - Occasional | | | 71 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | WNT10B CL E G H | 7480 | 12775 | OMIM:617073 | Tooth agenesis, selective, 8 | HP:0040283 - Occasional | | | 4 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | YY1 CL E G H | 7528 | 12856 | OMIM:617557 | Gabriele-De vries syndrome | | | | 7 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | YY1 CL E G H | 7528 | 12856 | ORPHA:506358 | Gabriele-de Vries syndrome | HP:0040283 - Occasional | | | 7 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | ZMPSTE24 CL E G H | 10269 | 12877 | ORPHA:1662 | Restrictive dermopathy | HP:0040281 - Very frequent | | | 83 | | |
HP:0045075 | HP:0045075 | Sparse eyebrow | 0 | ZMPSTE24 CL E G H | 10269 | 12877 | OMIM:275210 | Restrictive dermopathy, lethal | | | | 83 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | ATR CL E G H | 545 | 882 | OMIM:614564 | Cutaneous telangiectasia and cancer syndrome, familial | | | | 168 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | CDC42BPB CL E G H | 9578 | 1738 | OMIM:619841 | | | | | | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | COG6 CL E G H | 57511 | 18621 | ORPHA:363523 | Hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome | HP:0040282 - Frequent | | | 71 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | EDARADD CL E G H | 128178 | 14341 | OMIM:614941 | Ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive | . | | | 56 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | H4C5 CL E G H | 8367 | 4790 | OMIM:619950 | | | | | | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | HEPHL1 CL E G H | 341208 | 30477 | OMIM:261990 | PILI TORTI AND DEVELOPMENTAL DELAY | | | | | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | HNRNPK CL E G H | 3190 | 5044 | OMIM:616580 | Au-Kline syndrome | . | | | 8 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | IRX5 CL E G H | 10265 | 14361 | OMIM:611174 | Hamamy syndrome | . | | | 4 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | KAT5 CL E G H | 10524 | 5275 | OMIM:619103 | NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, SLEEP DISTURBANCE, AND BRAIN ABNORMALITIES; NEDFASB | | | | 1 | | |
HP:0045075 | HP:0025325 | Sparse medial eyebrow | 1 | KAT6A CL E G H | 7994 | 13013 | OMIM:616268 | Arboleda-Tham syndrome | | | | 34 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | KDM6A CL E G H | 7403 | 12637 | ORPHA:2322 | Kabuki syndrome | HP:0040281 - Very frequent | | | 53 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | KDM6A CL E G H | 7403 | 12637 | OMIM:300867 | Kabuki syndrome 2 | . | | | 53 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | KMT2D CL E G H | 8085 | 7133 | ORPHA:2322 | Kabuki syndrome | HP:0040281 - Very frequent | | | 660 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | KMT5B CL E G H | 51111 | 24283 | OMIM:617788 | Mental retardation, autosomal dominant 51 | | | | 2 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | KRT25 CL E G H | 147183 | 30839 | ORPHA:170 | Woolly hair | HP:0040283 - Occasional | | | 2 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | KRT71 CL E G H | 112802 | 28927 | ORPHA:170 | Woolly hair | HP:0040283 - Occasional | | | 1 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | KRT74 CL E G H | 121391 | 28929 | ORPHA:170 | Woolly hair | HP:0040283 - Occasional | | | 5 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | LIG4 CL E G H | 3981 | 6601 | ORPHA:235 | Dubowitz syndrome | HP:0040282 - Frequent | | | 88 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | LIPH CL E G H | 200879 | 18483 | ORPHA:170 | Woolly hair | HP:0040283 - Occasional | | | 12 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | LMBRD2 CL E G H | 92255 | 25287 | OMIM:619694 | DEVELOPMENTAL DELAY WITH VARIABLE NEUROLOGIC AND BRAIN ABNORMALITIES; DENBA | | | | | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | LPAR6 CL E G H | 10161 | 15520 | ORPHA:170 | Woolly hair | HP:0040283 - Occasional | | | 8 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | MAN1B1 CL E G H | 11253 | 6823 | OMIM:614202 | Rafiq syndrome | | | | 93 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | MESD CL E G H | 23184 | 13520 | OMIM:618644 | OSTEOGENESIS IMPERFECTA, TYPE XX; OI20 | | | | | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | NECTIN1 CL E G H | 5818 | 9706 | ORPHA:3253 | Cleft lip/palate-ectodermal dysplasia syndrome | HP:0040282 - Frequent | | | 4 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | NSUN2 CL E G H | 54888 | 25994 | ORPHA:235 | Dubowitz syndrome | HP:0040282 - Frequent | | | 84 | | |
HP:0045075 | HP:0025325 | Sparse medial eyebrow | 1 | NUP188 CL E G H | 23511 | 17859 | OMIM:618804 | SANDESTIG-STEFANOVA SYNDROME; SANDSTEF | | | | 4 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | PIGK CL E G H | 10026 | 8965 | OMIM:618879 | NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CEREBELLAR ATROPHY, WITH OR WITHOUT SEIZURES; NEDHCAS | | | | | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | PLXNA1 CL E G H | 5361 | 9099 | OMIM:619955 | | | | | | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | PPP1CB CL E G H | 5500 | 9282 | OMIM:617506 | Noonan syndrome-like disorder with loose anagen hair 2 | | | | 9 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | PQBP1 CL E G H | 10084 | 9330 | OMIM:309500 | Renpenning syndrome | . | | | 28 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | PURA CL E G H | 5813 | 9701 | ORPHA:314655 | Severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion | HP:0040282 - Frequent | | | 53 | | |
HP:0045075 | HP:0025325 | Sparse medial eyebrow | 1 | SIAH1 CL E G H | 6477 | 10857 | OMIM:619314 | BURATTI-HAREL SYNDROME; BURHAS | | | | | | |
HP:0045075 | HP:0025325 | Sparse medial eyebrow | 1 | SMARCA2 CL E G H | 6595 | 11098 | OMIM:601358 | Nicolaides-Baraitser syndrome | | | | 146 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | TBX3 CL E G H | 6926 | 11602 | OMIM:181450 | Ulnar-Mammary syndrome | . | | | 100 | | |
HP:0045075 | HP:0025325 | Sparse medial eyebrow | 1 | TCF4 CL E G H | 6925 | 11634 | OMIM:610954 | Pitt-Hopkins syndrome | | | | 241 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | TRPS1 CL E G H | 7227 | 12340 | OMIM:190350 | Trichorhinophalangeal syndrome, type I | . | | | 171 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | TRPS1 CL E G H | 7227 | 12340 | OMIM:190351 | Trichorhinophalangeal syndrome, type III | . | | | 171 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | TWIST2 CL E G H | 117581 | 20670 | ORPHA:1807 | Focal facial dermal dysplasia type III | HP:0040282 - Frequent | | | 7 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | USB1 CL E G H | 79650 | 25792 | OMIM:604173 | Poikiloderma with neutropenia | | | | 8 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | WDR26 CL E G H | 80232 | 21208 | ORPHA:513456 | Intellectual disability-seizures-abnormal gait-facial dysmorphism syndrome | HP:0040282 - Frequent | | | 8 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | WDR26 CL E G H | 80232 | 21208 | OMIM:617616 | Skraban-Deardorff syndrome | . | | | 8 | | |
HP:0045075 | HP:0005338 | Sparse lateral eyebrow | 1 | WLS CL E G H | 79971 | 30238 | OMIM:619648 | ZAKI SYNDROME; ZKS | | | | | | |