Wide nasal bridge

Symptom Information:

Symptom ID: HPO:0000431
Synonyms:
BROAD FLAT NASAL BRIDGE [HPO:0000431]
Broad nasal bridge [HPO:0000431]
Broad nasal root [HPO:0000431]
Broadened nasal bridge [HPO:0000431]
Nasal bridge broad [HPO:0000431]
Widened nasal bridge [HPO:0000431]
Broad nasal root [Orphanet:8390]
Wide nose (finding) [Orphanet:8090]
Wide nose [Orphanet:8090]
Broad flat nasal bridge [OMIM:Broad flat nasal bridge]
Broad nasal bridge [OMIM:Broad nasal bridge]
Broad nasal root [OMIM:Broad nasal root]
Broadened nasal bridge [OMIM:Broadened nasal bridge]
Nasal bridge broad [OMIM:Nasal bridge broad]
Wide nasal bridge [OMIM:Wide nasal bridge]
Widened nasal bridge [OMIM:Widened nasal bridge]
Broad nose/nasal bridge [Orphanet:8090]
Broad nasal bridge (95%) [OMIM:Broad nasal bridge (95%)]
Broad nasal bridge (97%) [OMIM:Broad nasal bridge (97%)]
Broad nasal bridge (in 1 family) [OMIM:Broad nasal bridge (in 1 family)]
Broad nasal bridge (in one family) [OMIM:Broad nasal bridge (in one family)]
Broad nasal bridge (in some patients) [OMIM:Broad nasal bridge (in some patients)]
Broad nasal bridge (uncommon) [OMIM:Broad nasal bridge (uncommon)]
Broad nasal bridge. [OMIM:Broad nasal bridge.]
Broad nasal root (2 patients) [OMIM:Broad nasal root (2 patients)]
Broad nasal root (reported in 1 patient) [OMIM:Broad nasal root (reported in 1 patient)]
Broad, flat nasal bridge [OMIM:Broad, flat nasal bridge]
Flat, broad nasal bridge [OMIM:Flat, broad nasal bridge]
Wide nasal bridge (1 family) [OMIM:Wide nasal bridge (1 family)]
Quality:
Cross references:
Orphanet:8390 "Broad nasal root" [Orphanet:8390]
Orphanet:8090 "Broad nose/nasal bridge" [Orphanet:8090]
OMIM: "Broad flat nasal bridge" [OMIM:Broad flat nasal bridge]
OMIM: "Broad nasal bridge" [OMIM:Broad nasal bridge]
OMIM: "Broad nasal root" [OMIM:Broad nasal root]
OMIM: "Broadened nasal bridge" [OMIM:Broadened nasal bridge]
OMIM: "Nasal bridge broad" [OMIM:Nasal bridge broad]
OMIM: "Wide nasal bridge" [OMIM:Wide nasal bridge]
OMIM: "Widened nasal bridge" [OMIM:Widened nasal bridge]
OMIM: "Broad nasal bridge (95%)" [OMIM:Broad nasal bridge (95%)]
OMIM: "Broad nasal bridge (97%)" [OMIM:Broad nasal bridge (97%)]
OMIM: "Broad nasal bridge (in 1 family)" [OMIM:Broad nasal bridge (in 1 family)]
OMIM: "Broad nasal bridge (in one family)" [OMIM:Broad nasal bridge (in one family)]
OMIM: "Broad nasal bridge (in some patients)" [OMIM:Broad nasal bridge (in some patients)]
OMIM: "Broad nasal bridge (uncommon)" [OMIM:Broad nasal bridge (uncommon)]
OMIM: "Broad nasal bridge." [OMIM:Broad nasal bridge.]
OMIM: "Broad nasal root (2 patients)" [OMIM:Broad nasal root (2 patients)]
OMIM: "Broad nasal root (reported in 1 patient)" [OMIM:Broad nasal root (reported in 1 patient)]
OMIM: "Broad, flat nasal bridge" [OMIM:Broad, flat nasal bridge]
OMIM: "Flat, broad nasal bridge" [OMIM:Flat, broad nasal bridge]
OMIM: "Wide nasal bridge (1 family)" [OMIM:Wide nasal bridge (1 family)]
UMLS:C0426421 "Wide nose" [Orphanet:8090]
Is a (Direct Parents):
HPO         Abnormality of the nasal bridge
Orphanet Abnormality of the nose
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the face(HPO:0000271)
                Abnormality of the nose(HPO:0000366)
                   Abnormality of the nasal bridge(HPO:0000422)
                      Wide nasal bridge(HPO:0000431)
MedDRA:
Database Frequency: 290 / 7739
Resource:

All diseases associated with this symptom:

15q24 microdeletion syndrome (Orphanet:94065)
1p36 deletion syndrome (Orphanet:1606)
20p12.3 microdeletion syndrome (Orphanet:261295)
2p15p16.1 microdeletion syndrome (Orphanet:261349)
3C syndrome (Orphanet:7)
3MC SYNDROME 2 (OMIM:265050)
3q29 microduplication (Orphanet:251038)
5p13 microduplication syndrome (Orphanet:329802)
6q25 microdeletion syndrome (Orphanet:251056)
8q12 microduplication syndrome (Orphanet:228399)
8q21.11 microdeletion syndrome (Orphanet:284160)
8q22.1 microdeletion syndrome (Orphanet:178303)
AARSKOG SYNDROME, AUTOSOMAL DOMINANT (OMIM:100050)
AARSKOG-SCOTT SYNDROME (OMIM:305400)
ALG3-CDG (Orphanet:79321)
AMASTIA, BILATERAL, WITH URETERAL TRIPLICATION AND DYSMORPHISM (OMIM:104350)
ARTHROGRYPOSIS, DISTAL, TYPE 2A (OMIM:193700)
AXENFELD-RIEGER SYNDROME, TYPE 1 (OMIM:180500)
AXENFELD-RIEGER SYNDROME, TYPE 2 (OMIM:601499)
Aarskog-Scott syndrome (Orphanet:915)
Acro-cardio-facial syndrome (Orphanet:2008)
Acro-fronto-facio-nasal dysostosis (Orphanet:1784)
Acrocallosal syndrome (Orphanet:36)
Acrofacial dysostosis, Rodriguez type (Orphanet:1788)
Acroosteolysis, dominant type (Orphanet:955)
Alar cartilages hypoplasia - coloboma - telecanthus (Orphanet:2007)
Alpha-thalassemia - intellectual deficit syndrome linked to chromosome 16 (Orphanet:98791)
Ankyloblepharon - ectodermal defects - cleft lip/palate (Orphanet:1071)
Atrioventricular defect - blepharophimosis -radial defects (Orphanet:1352)
Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
Autosomal dominant Robinow syndrome (Orphanet:3107)
Autosomal dominant spondylocostal dysostosis (Orphanet:1797)
Autosomal recessive Robinow syndrome (Orphanet:1507)
Autosomal recessive deafness-onychodystrophy syndrome (Orphanet:79500)
Autosomal recessive omodysplasia (Orphanet:93329)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
Axenfeld-Rieger syndrome (Orphanet:782)
BARAITSER-WINTER SYNDROME 1 (OMIM:243310)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
Baraitser-Winter syndrome (Orphanet:2995)
Beemer-Ertbruggen syndrome (Orphanet:1237)
Blepharophimosis - epicanthus inversus - ptosis (Orphanet:126)
Blepharophimosis - ptosis - esotropia - syndactyly - short stature (Orphanet:2057)
Blepharophimosis-intellectual deficit syndrome, MKB type (Orphanet:293707)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
Bohring-Opitz syndrome (Orphanet:97297)
Boomerang dysplasia (Orphanet:1263)
Brachydactyly - preaxial hallux varus (Orphanet:1278)
Brachymorphism - onychodysplasia - dysphalangism (Orphanet:1292)
Branchio-skeleto-genital syndrome (Orphanet:1299)
C syndrome (Orphanet:1308)
CARPENTER SYNDROME 2 (OMIM:614976)
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION (OMIM:601088)
CEDNIK syndrome (Orphanet:66631)
CHROMOSOME 16q22 DELETION SYNDROME (OMIM:614541)
CHROMOSOME 4q32.1-q32.2 TRIPLICATION SYNDROME (OMIM:613603)
CLN10 disease (Orphanet:228337)
COFS syndrome (Orphanet:1466)
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTALDELAY (OMIM:616266)
CORNELIA DE LANGE SYNDROME 4 (OMIM:614701)
CRANIODIAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT (OMIM:122860)
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE (OMIM:218400)
Carpenter-Waziri syndrome (Orphanet:93973)
Cartilage-hair hypoplasia (Orphanet:175)
Cerebro-facio-articular syndrome (Orphanet:314679)
Chondrodysplasia with joint dislocations, gPAPP type (Orphanet:280586)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Combined immunodeficiency with facio-oculo-skeletal anomalies (Orphanet:221139)
Combined oxidative phosphorylation defect type 14 (Orphanet:319519)
Congenital brain dysgenesis due to glutamine synthetase deficiency (Orphanet:71278)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
Congenital neuronal ceroid lipofuscinosis (Orphanet:168486)
Congenital pulmonary lymphangiectasia (Orphanet:2414)
Corpus callosum agenesis - neuronopathy (Orphanet:1496)
Craniodiaphyseal dysplasia (Orphanet:1513)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
Craniofaciofrontodigital syndrome (Orphanet:363705)
Craniofrontonasal dysplasia (Orphanet:1520)
Craniolenticulosutural dysplasia (Orphanet:50814)
Craniometaphyseal dysplasia (Orphanet:1522)
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies (Orphanet:221145)
Cystic fibrosis - gastritis - megaloblastic anemia (Orphanet:2575)
Dahlberg-Borer-Newcomer syndrome (Orphanet:1563)
Dandy-Walker malformation - postaxial polydactyly (Orphanet:1566)
De Barsy syndrome (Orphanet:2962)
Deafness - intellectual deficit, Martin-Probst type (Orphanet:85321)
Deafness with labyrinthine aplasia, microtia, and microdontia (Orphanet:90024)
Deafness-craniofacial syndrome (Orphanet:3241)
Dislocation of the hip - dysmorphism (Orphanet:2412)
Distal monosomy 10q (Orphanet:96148)
Distal monosomy 15q (Orphanet:1596)
Distal monosomy 9p (Orphanet:1642)
Duane retraction syndrome (Orphanet:233)
Dubowitz syndrome (Orphanet:235)
Dyssegmental dysplasia, Silverman-Handmaker type (Orphanet:1865)
ECTODERMAL DYSPLASIA WITH MENTAL RETARDATION AND SYNDACTYLY (OMIM:600906)
EHLERS-DANLOS SYNDROME, PROGEROID TYPE, 1 (OMIM:130070)
Ehlers-Danlos syndrome, progeroid type (Orphanet:75496)
Endocrine-cerebro-osteodysplasia syndrome (Orphanet:199332)
Epimetaphyseal skeletal dysplasia (Orphanet:1819)
FACIAL DYSMORPHISM WITH MULTIPLE MALFORMATIONS (OMIM:227255)
FANCONI ANEMIA, COMPLEMENTATION GROUP L (OMIM:614083)
FEINGOLD SYNDROME 1 (OMIM:164280)
FG SYNDROME 4 (OMIM:300422)
Faciocardiorenal syndrome (Orphanet:1973)
Fallot complex - intellectual deficit - growth delay (Orphanet:3304)
Familial benign copper deficiency (Orphanet:1551)
Feingold syndrome (Orphanet:1305)
Fibulo-ulnar hypoplasia - renal anomalies (Orphanet:2256)
Filippi syndrome (Orphanet:3255)
Flat face - microstomia - ear anomaly (Orphanet:1968)
Floating-Harbor syndrome (Orphanet:2044)
Fraser syndrome (Orphanet:2052)
Freeman-Sheldon syndrome (Orphanet:2053)
Frontometaphyseal dysplasia (Orphanet:1826)
Frontonasal dysplasia (Orphanet:250)
Frontonasal dysplasia with alopecia and genital anomaly (Orphanet:228390)
Frontonasal dysplasia-severe microphthalmia-severe facial clefting syndrome (Orphanet:306542)
Fryns syndrome (Orphanet:2059)
Genito-palato-cardiac syndrome (Orphanet:2075)
Glomerulonephritis - sparse hair - telangiectasis (Orphanet:2087)
Goldberg-Shprintzen megacolon syndrome (Orphanet:66629)
Gorlin syndrome (Orphanet:377)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
Growth delay due to insulin-like growth factor I resistance (Orphanet:73273)
HELSMOORTEL-VAN DER AA SYNDROME (OMIM:615873)
HISTIDINURIA DUE TO A RENAL TUBULAR DEFECT (OMIM:235830)
HUMERORADIAL SYNOSTOSIS WITH CRANIOFACIAL ANOMALIES (OMIM:236410)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 (OMIM:239300)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2 (OMIM:614749)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 4 (OMIM:615716)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 5 (OMIM:616025)
HYPERTELORISM AND OTHER FACIAL DYSMORPHISM, BRACHYDACTYLY, GENITALABNORMALITIES, MENTAL RETARDATION, AND RECURRENT INFLAMMATORY EPISODES (OMIM:614684)
Hall-Riggs syndrome (Orphanet:2107)
Hennekam syndrome (Orphanet:2136)
Hennekam-Beemer syndrome (Orphanet:2135)
Hereditary orotic aciduria (Orphanet:30)
Hermansky-Pudlak syndrome with neutropenia (Orphanet:183678)
Hirsutism - skeletal dysplasia - intellectual deficit (Orphanet:2156)
Histidinuria - renal tubular defect (Orphanet:2158)
Holmes-Gang syndrome (Orphanet:93970)
Hurler syndrome (Orphanet:93473)
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly (Orphanet:2180)
Hyperphosphatasia-intellectual deficiency syndrome (Orphanet:247262)
Hypertelorism, Teebi type (Orphanet:1519)
Hypertrichotic osteochondrodysplasia, Cantu type (Orphanet:1517)
Hypoglossia - hypodactyly (Orphanet:989)
IMMUNODEFICIENCY 26 WITH OR WITHOUT NEUROLOGIC ABNORMALITIES (OMIM:615966)
Imperforate oropharynx - costo vetebral anomalies (Orphanet:2759)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
Intellectual deficit, X-linked - seizures - psoriasis (Orphanet:3052)
Isolated trigonocephaly (Orphanet:3366)
Joubert syndrome 10 (OMIM:300804)
Joubert syndrome 3 (OMIM:608629)
Joubert syndrome with ocular defect (Orphanet:220493)
Juberg-Marsidi syndrome (Orphanet:93972)
Jung-Wolff-Back-Stahl syndrome (Orphanet:2321)
KAHRIZI SYNDROME (OMIM:612713)
Kabuki syndrome (Orphanet:2322)
Koolen-De Vries syndrome (Orphanet:96169)
LIG4 syndrome (Orphanet:99812)
Langer-Giedion syndrome (Orphanet:502)
Lathosterolosis (Orphanet:46059)
Leukocyte adhesion deficiency (Orphanet:2968)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 13 (OMIM:613192)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15 (OMIM:614202)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 45 (OMIM:615979)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 5 (OMIM:611091)
MICROPHTHALMIA, SYNDROMIC 12 (OMIM:615524)
MICROPHTHALMIA, SYNDROMIC 9 (OMIM:601186)
MOMO syndrome (Orphanet:2563)
Mandibulofacial dysostosis - macroblepharon - macrostomia (Orphanet:357158)
Matthew-Wood syndrome (Orphanet:2470)
Meckel syndrome, type 12 (OMIM:616258)
Megalocornea-intellectual deficit syndrome (Orphanet:2479)
Metaphyseal acroscyphodysplasia (Orphanet:1240)
Micro syndrome (Orphanet:2510)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Miller-Dieker syndrome (Orphanet:531)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Monosomy 18p (Orphanet:1598)
Monosomy 22q13 (Orphanet:48652)
Monosomy 5p (Orphanet:281)
Monosomy 9p (Orphanet:261112)
Mowat-Wilson syndrome (Orphanet:2152)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Mulibrey nanism (Orphanet:2576)
Mullerian derivatives - lymphangiectasia - polydactyly (Orphanet:1655)
Multicentric carpo-tarsal osteolysis with or without nephropathy (Orphanet:2774)
Nasal dermoid cyst (Orphanet:141103)
Nasopalpebral lipoma - coloboma - telecanthus (Orphanet:2399)
Neonatal adrenoleukodystrophy (Orphanet:44)
Neurological conditions associated with aminoacylase 1 deficiency (Orphanet:137754)
Non-distal monosomy 10q (Orphanet:1581)
Oculomaxillofacial dysostosis (Orphanet:1794)
Oculoosteocutaneous syndrome (Orphanet:2713)
Omodysplasia (Orphanet:2733)
Omphalocele syndrome, Shprintzen-Goldberg type (Orphanet:3164)
Opitz G/BBB syndrome (Orphanet:2745)
Orofaciodigital syndrome type 1 (Orphanet:2750)
Orofaciodigital syndrome type 2 (Orphanet:2751)
Orofaciodigital syndrome type 8 (Orphanet:2755)
Osteocraniostenosis (Orphanet:2763)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Otopalatodigital syndrome type 1 (Orphanet:90650)
PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER) (OMIM:614886)
PEROXISOME BIOGENESIS DISORDER 1B (OMIM:601539)
PEROXISOME BIOGENESIS DISORDER 2B (OMIM:202370)
POLYHYDRAMNIOS, MEGALENCEPHALY, AND SYMPTOMATIC EPILEPSY (OMIM:611087)
PONTOCEREBELLAR HYPOPLASIA, TYPE 10 (OMIM:615803)
Perlman syndrome (Orphanet:2849)
Peroxisomal acyl-CoA oxidase deficiency (Orphanet:2971)
Pfeiffer syndrome (Orphanet:710)
Phocomelia, Schinzel type (Orphanet:2879)
Piebaldism (Orphanet:2884)
Pilodental dysplasia - refractive errors (Orphanet:2892)
Pitt-Hopkins syndrome (Orphanet:2896)
Pontocerebellar hypoplasia type 7 (Orphanet:284339)
Pontocerebellar hypoplasia, type 9 (OMIM:615809)
Potocki-Shaffer syndrome (Orphanet:52022)
Pyruvate dehydrogenase E1-alpha deficiency (Orphanet:79243)
Qazi-Markouizos syndrome (Orphanet:3010)
ROBERTS SYNDROME (OMIM:268300)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Renpenning syndrome (Orphanet:3242)
Retinitis pigmentosa (Orphanet:791)
Rhizomelic chondrodysplasia punctata type 2 (Orphanet:309796)
Ring chromosome 1 (Orphanet:1437)
Ring chromosome 6 (Orphanet:1448)
Roberts syndrome (Orphanet:3103)
Rubinstein-Taybi syndrome (Orphanet:783)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
SCARF syndrome (Orphanet:3134)
SHORT syndrome (Orphanet:3163)
SIMOSA CRANIOFACIAL SYNDROME (OMIM:182150)
SLC35A2-CDG (Orphanet:356961)
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE (OMIM:614066)
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE (OMIM:613744)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA WITH CHARACTERISTIC FACIES (OMIM:600093)
STEEL SYNDROME (OMIM:615155)
Sclerosteosis (Orphanet:3152)
Sheldon-Hall syndrome (Orphanet:1147)
Short stature - heart defect - craniofacial anomalies (Orphanet:1088)
Short stature - wormian bones - dextrocardia (Orphanet:2863)
Sialidosis type 1 (Orphanet:812)
Sialuria (Orphanet:3166)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Skeletal dysplasia - intellectual deficit (Orphanet:1436)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Smith-Magenis syndrome (Orphanet:819)
Spondyloepiphyseal dysplasia, Cantu type (Orphanet:163654)
Spondylometaphyseal dysplasia, Golden type (Orphanet:168544)
Subaortic stenosis - short stature (Orphanet:3191)
TARP syndrome (Orphanet:2886)
THAI SYMPHALANGISM SYNDROME (OMIM:608028)
TMCO1 defect syndrome (Orphanet:228407)
TRISOMY 18-LIKE SYNDROME (OMIM:601161)
Tetrasomy 12p (Orphanet:884)
Thrombocytopenia - Robin sequence (Orphanet:3323)
Timothy syndrome (Orphanet:65283)
Toriello-Lacassie-Droste syndrome (Orphanet:3339)
Treacher-Collins syndrome (Orphanet:861)
Trigonocephaly - short stature - developmental delay (Orphanet:3369)
Trisomy 12p (Orphanet:1699)
Trisomy 8q (Orphanet:1752)
VAN MALDERGEM SYNDROME 1 (OMIM:601390)
VAN MALDERGEM SYNDROME 2 (OMIM:615546)
VERHEIJ SYNDROME (OMIM:615583)
Velo-facial-skeletal syndrome (Orphanet:3424)
W syndrome (Orphanet:2804)
WAARDENBURG SYNDROME, TYPE 2A (OMIM:193510)
WARBURG MICRO SYNDROME 4 (OMIM:615663)
Waardenburg syndrome (Orphanet:3440)
Waardenburg syndrome type 1 (Orphanet:894)
Waardenburg syndrome type 2 (Orphanet:895)
White matter hypoplasia - corpus callosum agenesis - intellectual deficit (Orphanet:3207)
Wolf-Hirschhorn syndrome (Orphanet:280)
Wrinkly skin syndrome (Orphanet:2834)
X-linked Opitz G/BBB syndrome (Orphanet:306597)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)
X-linked intellectual deficit, Najm type (Orphanet:163937)
X-linked lissencephaly with abnormal genitalia (Orphanet:452)
Zechi-Ceide syndrome (Orphanet:217017)
Zellweger-like syndrome without peroxisomal anomalies (Orphanet:50812)
Zimmermann-Laband syndrome (Orphanet:3473)
Zlotogora-Ogur syndrome (Orphanet:3253)
Zunich-Kaye syndrome (Orphanet:3474)