| Disease Browser
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Parent Node:
 Abnormalities, Multiple (D000015) |
Parent Node:
Craniofacial Abnormalities (D019465) |
Parent Node:
Dwarfism (D004392) |
..Starting node
.. Seckel like syndrome type Buebel (C537532)
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Child Nodes:
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Sister Nodes: |
..Aarskog Syndrome (C535331)  1
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..Abuse dwarfism syndrome (C535569)
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..Achondroplasia (D000130) 21
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..Acromesomelic dysplasia (C535658) 1
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..Acromesomelic dysplasia Campailla-Martinelli type (C535659)
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..Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus (C565968)
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..Alopecia contractures dwarfism mental retardation (C537051)
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..Amino Aciduria with Mental Deficiency, Dwarfism, Muscular Dystrophy, Osteoporosis, and Acidosis (C565960)
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..Anauxetic dysplasia (C538256)
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..Astley-Kendall syndrome (C535392)
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..Asymmetric Short Stature Syndrome (C566248)
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..ATELOSTEOGENESIS, TYPE III (OMIM:108721)
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..Bangstad syndrome (C537902)
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..Bird headed dwarfism Montreal type (C535448)
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..Boomerang dysplasia (C536573)
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..Brachydactylous dwarfism Mseleni type (C537086)
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..Brachymetapody-Anodontia-Hypotrichosis-Albinoidism (C565893)
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..Brunoni syndrome (C537408)
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..Bullous Dystrophy, Hereditary Macular Type (C563065)
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..Cantu Sanchez-Corona Fragoso syndrome (C535571)
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..Chondrodysplasia Calcificans Metaphysealis (C565855)
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..Chondrodysplasia, Megarbane-Dagher-Melki Type (C567644)
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..Cockayne Syndrome (D003057) 6
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..Congenital Hypothyroidism (D003409) 17
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..De Sanctis-Cacchione syndrome (C535992)
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..Desbuquois syndrome (C535943)
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..Diastrophic dysplasia (C536170)
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..Diastrophic Dysplasia, Broad Bone-Platyspondylic Variant (C565626)
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..Disproportionate Short Stature with Ptosis and Valvular Heart Lesions (C565094)
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..Dwarfism stiff joint ocular abnormalities (C535724)
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..Dwarfism tall vertebrae (C535725)
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..Dwarfism, Familial, With Muscle Spasms (C563447)
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..Dwarfism, Levi Type (C565081)
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..Dwarfism, Low-Birth-Weight Type, with Unresponsiveness to Growth Hormone (C565615)
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..Dwarfism, Pituitary (D004393) 11
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..Dwarfism, Proportionate, with Hip Dislocation (C565614)
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..Dyggve-Melchior-Clausen syndrome (C535726)
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..Dyssegmental dysplasia (C537998)
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..Dyssegmental Dysplasia with Glaucoma (C563290)
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..Fibrochondrogenesis (C562524)
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..Gerodermia osteodysplastica (C537799)
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..Growth Retardation, Developmental Delay, Coarse Facies, And Early Death (C567856)
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..Hadziselimovic Syndrome (C567850)
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..Hypochondroplasia (C562937)
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..Ichthyosis, mental retardation, dwarfism, and renal impairment (C536274)
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..Isolated Growth Hormone Deficiency, Type IB (C567564)
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..Kenny Caffey syndrome (C537020)
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..Keratosis follicularis dwarfism cerebral atrophy (C536158)
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..Kniest dysplasia (C537207)
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..Laplane Fontaine Lagardere syndrome (C537869)
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..Laron Syndrome (D046150) 1
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..Megaepiphyseal dwarfism (C536140) 1
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..Mental retardation, macrocephaly, short stature and craniofacial dysmorphism (C537453)
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..Mental Retardation, Short Stature, Facial Anomalies, and Joint Dislocations (C565248)
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..Mesomelic Dwarfism of Hypoplastic Tibia and Radius Type (C563589)
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..Mesomelic dwarfism Reinhardt Pfeiffer type (C537349)
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..Metatropic dwarfism (C537356)
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..Metatropic Dwarfism, Type II (C581628)
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..Microcephalic osteodysplastic primordial dwarfism, type 1 (C537577)
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..Microcephalic osteodysplastic primordial dwarfism, type 3 (C537320)
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..Microcephalic Osteodysplastic Primordial Dwarfism, Type II (C565898)
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..Microcephalic primordial dwarfism Toriello type (C537321)
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..Miller-McKusick-Malvaux-Syndrome (3M Syndrome) (C535314)
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..Mollica Pavone Antener syndrome (C535809)
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..Mulibrey Nanism (D050336) 1
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..Nievergelt syndrome (C536120)
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..Oculopalatocerebral Syndrome (C564935)
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..Oliver-McFarlane syndrome (C536554)
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..Parastremmatic dwarfism (C537172)
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..Pseudodiastrophic dysplasia (C535826)
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..Rapadilino syndrome (C535288)
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..Robinow Syndrome, Autosomal Dominant (C562492)
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..Rommen Mueller Sybert syndrome (C535871)
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..Ruvalcaba Syndrome (C579395)
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..Seckel like syndrome type Buebel (C537532)
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..Seckel syndrome 1 (C537533)
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..Seckel syndrome 2 (C537534)
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..Seckel Syndrome 3 (C563881)
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..SECKEL SYNDROME 4 (OMIM:613676)
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..Short limb dwarfism Al Gazali type (C537598)
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..Short Stature And Facioauriculothoracic Malformations (C566457)
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..Short Stature, Mental Retardation, Callosal Agenesis, Heminasal Hypoplasia, Microphthalmia, And Atypical Clefting (C566989)
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..Short Stature-Obesity Syndrome (C564821)
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..Silver-Russell Syndrome (D056730) 1
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..Singh Chhaparwal Dhanda syndrome (C537341)
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..Spondyloepiphyseal dysplasia tarda, Toledo type (C535787)
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..Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type (C564794)
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..Synovial Chondromatosis, Familial, with Dwarfism (C566087)
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..Thoraco limb dysplasia Rivera type (C536516)
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..Thoracomelic Dysplasia (C564773)
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..Three M Syndrome 2 (C567862)
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..Tryptophanuria With Dwarfism (C562658)
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..Weill-Marchesani Syndrome (D056846)
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..Weill-Marchesani-Like Syndrome (C567710)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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