Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandAbnormalities, Multiple (D000015)
Parent Node:
expandFetal Growth Retardation (D005317)
..Starting node
..expandSharma Kapoor Ramji syndrome (C537595)

       Child Nodes:



 Sister Nodes: 
..expandBowen-Conradi syndrome (C537081)
..expandCamptodactyly syndrome Guadalajara type 2 (C537971)
..expandCartwright Nelson Fryns syndrome (C535917)
..expandCraniomicromelic Syndrome (C566522)
..expandDiabetes Mellitus, Permanent Neonatal, with Cerebellar Agenesis (C563796)
..expandFetal akinesia syndrome, X-linked (C537921)
..expandFinnish lethal neonatal metabolic syndrome (C537934)
..expandGranddad Syndrome (C564211)
..expandHoloprosencephaly with Fetal Akinesia/Hypokinesia Sequence (C564409)
..expandHoyeraal Hreidarsson syndrome (C536068)
..expandIntrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, And Genital Anomalies (C564543)
..expandLambotte syndrome (C537549)
..expandMicrocephalic osteodysplastic primordial dwarfism, type 1 (C537577)
..expandMicrocephalic osteodysplastic primordial dwarfism, type 3 (C537320)
..expandMicrocephalic Osteodysplastic Primordial Dwarfism, Type II (C565898)
..expandMicrocephaly, Severe, with Skeletal Anomalies including Posterior Rib-Gap Defects (C566377)
..expandNeu Laxova syndrome (C536405)
..expandProgeroid syndrome, neonatal (C536423)
..expandRay Peterson Scott syndrome (C535292)
..expandSECKEL SYNDROME 4 (OMIM:613676)
..expandSharma Kapoor Ramji syndrome (C537595)
..expandShort stature and locking fingers (C537603)
..expandThymic-Renal-Anal-Lung dysplasia (C536907)
..expandTrichohepatoenteric Syndrome (C565627)
..expandWoods Leversha Rogers syndrome (C536744)
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:10176
Name:Sharma Kapoor Ramji syndrome
Definition:
Alternative IDs:
ParentIDs:MESH:D000015|MESH:D005317
TreeNumbers:C13.703.277.370/C537595 |C16.131.077/C537595 |C16.300.390/C537595 |C23.550.393.450/C537595
Synonyms:
Slim Mappings:Congenital abnormality|Fetal disease|Pathology (process)|Pregnancy complication
Reference: MedGen: C537595
MeSH: C537595
OMIM:

Genes:
Phenotypes
Disease Causing ClinVar Variants