The following pages link to Dysmorphic feature
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Congenital disorder of glycosylation (links | edit)
- Teratology (links | edit)
- Megalencephaly (links | edit)
- Plagiocephaly (links | edit)
- Unibrow (links | edit)
- Methylmalonic acidemias (links | edit)
- Polymicrogyria (links | edit)
- Hypotonia (links | edit)
- Failure to thrive (links | edit)
- Jacobsen syndrome (links | edit)
- DSCAM (links | edit)
- Small supernumerary marker chromosome (links | edit)
- Microtia (links | edit)
- Tafazzin (links | edit)
- 3 hydroxyisobutyric aciduria (links | edit)
- Monosomy 9p (links | edit)
- XXXXY syndrome (links | edit)
- Macrodontia (tooth) (links | edit)
- Dysmorphism (redirect page) (links | edit)
- Leigh syndrome (links | edit)
- The Gumps (links | edit)
- Hemeralopia (links | edit)
- Trisomy 9 (links | edit)
- D-bifunctional protein deficiency (links | edit)
- Young–Simpson syndrome (links | edit)
- PHF8 (links | edit)
- 8p23.1 duplication syndrome (links | edit)
- Cataract-microcornea syndrome (links | edit)
- Sanjad–Sakati syndrome (links | edit)
- Trisomy X (links | edit)
- Porencephaly-cerebellar hypoplasia-internal malformations syndrome (links | edit)
- 15q overgrowth syndrome (links | edit)
- User:Asofiav25/Trisomy X (links | edit)
- Aldolase A deficiency (links | edit)
- SMC1A (links | edit)
- EIF5A (links | edit)
- SMC3 (links | edit)
- USP9X (links | edit)
- COX4I1 (links | edit)
- Dysmorphic (redirect page) (links | edit)
- B. Kliban (links | edit)
- Inward-rectifier potassium channel (links | edit)
- Henmaru Machino (links | edit)
- Gonadal dysgenesis (links | edit)
- Electroneutral cation-Cl (links | edit)
- Mevalonate kinase deficiency (links | edit)
- ST3GAL5 (links | edit)
- WDR37 (links | edit)
- Keutel syndrome (links | edit)
- Perlman syndrome (links | edit)
- Sotos syndrome (links | edit)
- PAM16 (links | edit)
- Cohen–Gibson syndrome (links | edit)
- TRPM3-related neurodevelopmental disorder (links | edit)
- Bachmann-Bupp syndrome (links | edit)
- RNU4-2 syndrome (links | edit)
- User:Hetal05/sandbox (links | edit)
- Acrocallosal syndrome (links | edit)
- Dysmorphy (redirect page) (links | edit)
- Tricho-hepato-enteric syndrome (links | edit)
- Lathosterolosis (links | edit)
- Wilson–Turner syndrome (links | edit)
- Facial dysmorphism (redirect page) (links | edit)
- Sanfilippo syndrome (links | edit)
- Ring chromosome (links | edit)
- Copenhagen disease (links | edit)
- Monosomy 9p (links | edit)
- POLD1 (links | edit)
- COX7B (links | edit)
- 3-M syndrome (links | edit)
- Wrinkly skin syndrome (links | edit)
- CEDNIK syndrome (links | edit)
- 2q37 monosomy (links | edit)
- STAR syndrome (links | edit)
- Hand and foot deformity with flat facies (links | edit)
- Zaki syndrome (links | edit)
- Cardiospondylocarpofacial syndrome (links | edit)
- CACNA1C-related disorders (links | edit)
- User:Rpatel76/sandbox (links | edit)
- User:Imunoz02/sandbox (links | edit)
- 8p23.1 duplication syndrome (links | edit)
- 3q29 microdeletion syndrome (links | edit)
- Organic anion transporter 1 (links | edit)
- Hyperphosphatasia with mental retardation syndrome (links | edit)
- Cernunnos deficiency (links | edit)
- Pontocerebellar hypoplasia (links | edit)
- Progeroid syndromes (links | edit)
- Wiedemann–Rautenstrauch syndrome (links | edit)
- Ogden syndrome (links | edit)
- Male genital examination (links | edit)
- DNAJC30 (links | edit)
- COACH syndrome (links | edit)
- UQCC2 (links | edit)
- TMEM70 (links | edit)
- Dysmorphic features (redirect page) (links | edit)
- Small supernumerary marker chromosome (links | edit)
- 22q13 deletion syndrome (links | edit)
- Micrognathism (links | edit)
- GestaltMatcher (links | edit)
- Misplaced Pages:Featured article candidates/Trisomy X/archive1 (links | edit)
- Misplaced Pages:Featured article candidates/Archived nominations/September 2021 (links | edit)
- C4orf51 (links | edit)
- Microcephaly albinism digital anomalies syndrome (links | edit)
- Tetrasomy X (links | edit)