Ontomatica – ChEMATIC (Wedge)

The current query selects 783 items in 91 groups, which could be too many to show at once. If you are sure you want to see them all, you can proceed to see the entire category, 'or select a more specific subcategory of "Dwarfism [MESH:D004392]" below.

Subcategories in Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Genetic Diseases, Inborn [MESH:D030342] > Dwarfism [MESH:D004392]:
(jump to A - B - C - D - F - G - H - I - K - L - M - N - O - P - R - S - T - W)

- A -
Aarskog Syndrome [MESH:C535331] (18)
Abuse dwarfism syndrome [MESH:C535569] (1)
Achondroplasia [MESH:D000130] (196)
Acromesomelic dysplasia Campailla-Martinelli type [MESH:C535659] (1)
Acromesomelic dysplasia [MESH:C535658] (1)
Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus [MESH:C565968] (1)
Alopecia contractures dwarfism mental retardation [MESH:C537051] (1)
Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis [MESH:C565960] (1)
Anauxetic dysplasia [MESH:C538256] (4)
Asthma, Short Stature, and Elevated IgA [MESH:C565934] (1)
Astley-Kendall syndrome [MESH:C535392] (1)
Asymmetric Short Stature Syndrome [MESH:C566248] (1)

- B -
Bangstad syndrome [MESH:C537902] (1)
Bird headed dwarfism Montreal type [MESH:C535448] (1)
Boomerang dysplasia [MESH:C536573] (44)
Brachydactylous dwarfism Mseleni type [MESH:C537086] (1)
Brachymetapody-Anodontia-Hypotrichosis-Albinoidism [MESH:C565893] (1)
Brunoni syndrome [MESH:C537408] (1)
Bullous Dystrophy, Hereditary Macular Type [MESH:C563065] (1)

- C -
Cantu Sanchez-Corona Fragoso syndrome [MESH:C535571] (1)
Chondrodysplasia Calcificans Metaphysealis [MESH:C565855] (1)
Chondrodysplasia, Megarbane-Dagher-Melki Type [MESH:C567644] (1)
Cockayne Syndrome [MESH:D003057] (107)
Congenital Hypothyroidism [MESH:D003409] (266)

- D -
De Sanctis-Cacchione syndrome [MESH:C535992] (27)
Desbuquois syndrome [MESH:C535943] (20)
Diastrophic Dysplasia, Broad Bone-Platyspondylic Variant [MESH:C565626] (1)
Diastrophic dysplasia [MESH:C536170] (34)
Disproportionate Short Stature with Ptosis and Valvular Heart Lesions [MESH:C565094] (1)
Dwarfism stiff joint ocular abnormalities [MESH:C535724] (1)
Dwarfism tall vertebrae [MESH:C535725] (1)
Dwarfism, Familial, With Muscle Spasms [MESH:C563447] (1)
Dwarfism, Levi Type [MESH:C565081] (1)
Dwarfism, Low-Birth-Weight Type, with Unresponsiveness to Growth Hormone [MESH:C565615] (1)
Dwarfism, Proportionate, with Hip Dislocation [MESH:C565614] (1)
Dyggve-Melchior-Clausen syndrome [MESH:C535726] (19)
Dyssegmental Dysplasia with Glaucoma [MESH:C563290] (1)
Dyssegmental dysplasia [MESH:C537998] (21)

- F -
Fibrochondrogenesis [MESH:C562524] (1)

- G -
Gerodermia osteodysplastica [MESH:C537799] (12)
Growth Retardation, Developmental Delay, Coarse Facies, And Early Death [MESH:C567856] (12)

- H -
Hadziselimovic Syndrome [MESH:C567850] (1)
Hypochondroplasia [MESH:C562937] (66)

- I -
Ichthyosis, mental retardation, dwarfism, and renal impairment [MESH:C536274] (1)
Isolated Growth Hormone Deficiency, Type IB [MESH:C567564] (140)

- K -
Kenny Caffey syndrome [MESH:C537020] (24)
Keratosis follicularis dwarfism cerebral atrophy [MESH:C536158] (1)
Kniest dysplasia [MESH:C537207] (89)

- L -
Laplane Fontaine Lagardere syndrome [MESH:C537869] (1)
Laron Syndrome [MESH:D046150] (91)

- M -
Megaepiphyseal dwarfism [MESH:C536140] (1)
Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations [MESH:C565248] (1)
Mental retardation, macrocephaly, short stature and craniofacial dysmorphism [MESH:C537453] (1)
Mesomelic Dwarfism of Hypoplastic Tibia and Radius Type [MESH:C563589] (1)
Mesomelic dwarfism Reinhardt Pfeiffer type [MESH:C537349] (1)
Metatropic Dwarfism, Type II [MESH:C581628] (1)
Metatropic dwarfism [MESH:C537356] (39)
Microcephalic Osteodysplastic Primordial Dwarfism, Type II [MESH:C565898] (7)
Microcephalic osteodysplastic primordial dwarfism, type 1 [MESH:C537577] (1)
Microcephalic osteodysplastic primordial dwarfism, type 3 [MESH:C537320] (1)
Microcephalic primordial dwarfism Toriello type [MESH:C537321] (1)
Miller-McKusick-Malvaux-Syndrome (3M Syndrome) [MESH:C535314] (1)
Mollica Pavone Antener syndrome [MESH:C535809] (1)
Mulibrey Nanism [MESH:D050336] (18)

- N -
Nievergelt syndrome [MESH:C536120] (1)

- O -
Oculopalatocerebral Syndrome [MESH:C564935] (1)
Oliver-McFarlane syndrome [MESH:C536554] (1)

- P -
Parastremmatic dwarfism [MESH:C537172] (39)
Pseudodiastrophic dysplasia [MESH:C535826] (1)

- R -
Rapadilino syndrome [MESH:C535288] (30)
Robinow Syndrome, Autosomal Dominant [MESH:C562492] (1)
Rommen Mueller Sybert syndrome [MESH:C535871] (1)
Ruvalcaba Syndrome [MESH:C579395] (1)

- S -
Seckel Syndrome 3 [MESH:C563881] (1)
Seckel like syndrome type Buebel [MESH:C537532] (1)
Seckel syndrome 1 [MESH:C537533] (63)
Seckel syndrome 2 [MESH:C537534] (7)
Short Stature And Facioauriculothoracic Malformations [MESH:C566457] (1)
Short Stature, Mental Retardation, Callosal Agenesis, Heminasal Hypoplasia, Microphthalmia, And Atypical Clefting [MESH:C566989] (1)
Short Stature-Obesity Syndrome [MESH:C564821] (1)
Short limb dwarfism Al Gazali type [MESH:C537598] (1)
Silver-Russell Syndrome [MESH:D056730] (142)
Singh Chhaparwal Dhanda syndrome [MESH:C537341] (1)
Spondyloepiphyseal dysplasia tarda, Toledo type [MESH:C535787] (1)
Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type [MESH:C564794] (29)
Synovial Chondromatosis, Familial, with Dwarfism [MESH:C566087] (1)

- T -
Thoraco limb dysplasia Rivera type [MESH:C536516] (1)
Thoracomelic Dysplasia [MESH:C564773] (1)
Three M Syndrome 2 [MESH:C567862] (22)
Tryptophanuria With Dwarfism [MESH:C562658] (1)

- W -
Weill-Marchesani-Like Syndrome [MESH:C567710] (5)